○chromosomal test for leukemia/malignant lymphomas
TEST NAME
SPECIMEN REQUIREMENT (mL)
CONTAINER
CAP COLOR
STORE TEMPERATURE (STABILITY)
TURNAROUND TIME (DAY)
METHODOLOGY
REFERENCE RANGE (UNIT)
Chromosome G-Banding
bone marrow aspirate
1.0
H00
8-14
G-band
(Various) Band Culture lymphocytes or bone marrow cells, and fix metaphase cells. This method then stains the chromosomes with a dye to create a striped pattern (band), and analyzes the distribution and density of the band. G-Banding, which performs Giemsa staining after treatment with trypsin solution, C-Banding, which performs Giemsa staining after treatment with HCI, Ba (OH) 2, 2×SCC, these include Q-Banding, which involves staining with quinacrine mustard and then observing with a fluorescence microscope, and high-precision banding, which uses mitotic images from the end of prophase to the beginning of metaphase, and observes a larger number of bands than usual.
Chromosome G-Banding
Blood (heparin added)
5.0
PH5
8-14
G-band
(Various) Band Culture lymphocytes or bone marrow cells, and fix metaphase cells. This method then stains the chromosomes with a dye to create a striped pattern (band), and analyzes the distribution and density of the band. G-Banding, which performs Giemsa staining after treatment with trypsin solution, C-Banding, which performs Giemsa staining after treatment with HCI, Ba (OH) 2, 2×SCC, these include Q-Banding, which involves staining with quinacrine mustard and then observing with a fluorescence microscope, and high-precision banding, which uses mitotic images from the end of prophase to the beginning of metaphase, and observes a larger number of bands than usual.
Chromosome SKY (blood disorders)
bone marrow aspirate
1.0
H00
25-29
FISH
(Various) Band Culture lymphocytes or bone marrow cells, and fix metaphase cells. This method then stains the chromosomes with a dye to create a striped pattern (band), and analyzes the distribution and density of the band. G-Banding, which performs Giemsa staining after treatment with trypsin solution, C-Banding, which performs Giemsa staining after treatment with HCI, Ba (OH) 2, 2×SCC, these include Q-Banding, which involves staining with quinacrine mustard and then observing with a fluorescence microscope, and high-precision banding, which uses mitotic images from the end of prophase to the beginning of metaphase, and observes a larger number of bands than usual.
Chromosome SKY (blood disorders)
Blood (heparin added)
5.0
PH5
25-29
FISH
(Various) Band Culture lymphocytes or bone marrow cells, and fix metaphase cells. This method then stains the chromosomes with a dye to create a striped pattern (band), and analyzes the distribution and density of the band. G-Banding, which performs Giemsa staining after treatment with trypsin solution, C-Banding, which performs Giemsa staining after treatment with HCI, Ba (OH) 2, 2×SCC, these include Q-Banding, which involves staining with quinacrine mustard and then observing with a fluorescence microscope, and high-precision banding, which uses mitotic images from the end of prophase to the beginning of metaphase, and observes a larger number of bands than usual.
TCF3-PBX1 t(1;19) translocation
bone marrow aspirate
1.0
H00
7-10
FISH
(Various) Band Culture lymphocytes or bone marrow cells, and fix metaphase cells. This method then stains the chromosomes with a dye to create a striped pattern (band), and analyzes the distribution and density of the band. G-Banding, which performs Giemsa staining after treatment with trypsin solution, C-Banding, which performs Giemsa staining after treatment with HCI, Ba (OH) 2, 2×SCC, these include Q-Banding, which involves staining with quinacrine mustard and then observing with a fluorescence microscope, and high-precision banding, which uses mitotic images from the end of prophase to the beginning of metaphase, and observes a larger number of bands than usual.
TCF3-PBX1 t(1;19) translocation
Blood (heparin added)
5.0
PH5
7-10
FISH
(Various) Band Culture lymphocytes or bone marrow cells, and fix metaphase cells. This method then stains the chromosomes with a dye to create a striped pattern (band), and analyzes the distribution and density of the band. G-Banding, which performs Giemsa staining after treatment with trypsin solution, C-Banding, which performs Giemsa staining after treatment with HCI, Ba (OH) 2, 2×SCC, these include Q-Banding, which involves staining with quinacrine mustard and then observing with a fluorescence microscope, and high-precision banding, which uses mitotic images from the end of prophase to the beginning of metaphase, and observes a larger number of bands than usual.
CKS1B 1q21 amplification
bone marrow aspirate
1.0
H00
7-10
FISH
(Various) Band Culture lymphocytes or bone marrow cells, and fix metaphase cells. This method then stains the chromosomes with a dye to create a striped pattern (band), and analyzes the distribution and density of the band. G-Banding, which performs Giemsa staining after treatment with trypsin solution, C-Banding, which performs Giemsa staining after treatment with HCI, Ba (OH) 2, 2×SCC, these include Q-Banding, which involves staining with quinacrine mustard and then observing with a fluorescence microscope, and high-precision banding, which uses mitotic images from the end of prophase to the beginning of metaphase, and observes a larger number of bands than usual.
CKS1B 1q21 amplification
Blood (heparin added)
5.0
PH5
7-10
FISH
(Various) Band Culture lymphocytes or bone marrow cells, and fix metaphase cells. This method then stains the chromosomes with a dye to create a striped pattern (band), and analyzes the distribution and density of the band. G-Banding, which performs Giemsa staining after treatment with trypsin solution, C-Banding, which performs Giemsa staining after treatment with HCI, Ba (OH) 2, 2×SCC, these include Q-Banding, which involves staining with quinacrine mustard and then observing with a fluorescence microscope, and high-precision banding, which uses mitotic images from the end of prophase to the beginning of metaphase, and observes a larger number of bands than usual.
ALK 2p23 translocation
lymph nodes
5×5×5mm
H00
7-10
FISH
(Various) Band Culture lymphocytes or bone marrow cells, and fix metaphase cells. This method then stains the chromosomes with a dye to create a striped pattern (band), and analyzes the distribution and density of the band. G-Banding, which performs Giemsa staining after treatment with trypsin solution, C-Banding, which performs Giemsa staining after treatment with HCI, Ba (OH) 2, 2×SCC, these include Q-Banding, which involves staining with quinacrine mustard and then observing with a fluorescence microscope, and high-precision banding, which uses mitotic images from the end of prophase to the beginning of metaphase, and observes a larger number of bands than usual.
ALK 2p23 translocation
bone marrow aspirate
1.0
H00
7-10
FISH
(Various) Band Culture lymphocytes or bone marrow cells, and fix metaphase cells. This method then stains the chromosomes with a dye to create a striped pattern (band), and analyzes the distribution and density of the band. G-Banding, which performs Giemsa staining after treatment with trypsin solution, C-Banding, which performs Giemsa staining after treatment with HCI, Ba (OH) 2, 2×SCC, these include Q-Banding, which involves staining with quinacrine mustard and then observing with a fluorescence microscope, and high-precision banding, which uses mitotic images from the end of prophase to the beginning of metaphase, and observes a larger number of bands than usual.
ALK 2p23 translocation
Blood (heparin added)
5.0
PH5
7-10
FISH
(Various) Band Culture lymphocytes or bone marrow cells, and fix metaphase cells. This method then stains the chromosomes with a dye to create a striped pattern (band), and analyzes the distribution and density of the band. G-Banding, which performs Giemsa staining after treatment with trypsin solution, C-Banding, which performs Giemsa staining after treatment with HCI, Ba (OH) 2, 2×SCC, these include Q-Banding, which involves staining with quinacrine mustard and then observing with a fluorescence microscope, and high-precision banding, which uses mitotic images from the end of prophase to the beginning of metaphase, and observes a larger number of bands than usual.
GATA2-MECOM inv(3) inversion,t(3;3) translocation
bone marrow aspirate
1.0
H00
7-10
FISH
(Various) Band Culture lymphocytes or bone marrow cells, and fix metaphase cells. This method then stains the chromosomes with a dye to create a striped pattern (band), and analyzes the distribution and density of the band. G-Banding, which performs Giemsa staining after treatment with trypsin solution, C-Banding, which performs Giemsa staining after treatment with HCI, Ba (OH) 2, 2×SCC, these include Q-Banding, which involves staining with quinacrine mustard and then observing with a fluorescence microscope, and high-precision banding, which uses mitotic images from the end of prophase to the beginning of metaphase, and observes a larger number of bands than usual.
GATA2-MECOM inv(3) inversion,t(3;3) translocation
Blood (heparin added)
5.0
PH5
7-10
FISH
(Various) Band Culture lymphocytes or bone marrow cells, and fix metaphase cells. This method then stains the chromosomes with a dye to create a striped pattern (band), and analyzes the distribution and density of the band. G-Banding, which performs Giemsa staining after treatment with trypsin solution, C-Banding, which performs Giemsa staining after treatment with HCI, Ba (OH) 2, 2×SCC, these include Q-Banding, which involves staining with quinacrine mustard and then observing with a fluorescence microscope, and high-precision banding, which uses mitotic images from the end of prophase to the beginning of metaphase, and observes a larger number of bands than usual.
BCL6 3q27 translocation
lymph nodes
5×5×5mm
H00
7-10
FISH
(Various) Band Culture lymphocytes or bone marrow cells, and fix metaphase cells. This method then stains the chromosomes with a dye to create a striped pattern (band), and analyzes the distribution and density of the band. G-Banding, which performs Giemsa staining after treatment with trypsin solution, C-Banding, which performs Giemsa staining after treatment with HCI, Ba (OH) 2, 2×SCC, these include Q-Banding, which involves staining with quinacrine mustard and then observing with a fluorescence microscope, and high-precision banding, which uses mitotic images from the end of prophase to the beginning of metaphase, and observes a larger number of bands than usual.
BCL6 3q27 translocation
bone marrow aspirate
1.0
H00
7-10
FISH
(Various) Band Culture lymphocytes or bone marrow cells, and fix metaphase cells. This method then stains the chromosomes with a dye to create a striped pattern (band), and analyzes the distribution and density of the band. G-Banding, which performs Giemsa staining after treatment with trypsin solution, C-Banding, which performs Giemsa staining after treatment with HCI, Ba (OH) 2, 2×SCC, these include Q-Banding, which involves staining with quinacrine mustard and then observing with a fluorescence microscope, and high-precision banding, which uses mitotic images from the end of prophase to the beginning of metaphase, and observes a larger number of bands than usual.
BCL6 3q27 translocation
Blood (heparin added)
5.0
PH5
7-10
FISH
(Various) Band Culture lymphocytes or bone marrow cells, and fix metaphase cells. This method then stains the chromosomes with a dye to create a striped pattern (band), and analyzes the distribution and density of the band. G-Banding, which performs Giemsa staining after treatment with trypsin solution, C-Banding, which performs Giemsa staining after treatment with HCI, Ba (OH) 2, 2×SCC, these include Q-Banding, which involves staining with quinacrine mustard and then observing with a fluorescence microscope, and high-precision banding, which uses mitotic images from the end of prophase to the beginning of metaphase, and observes a larger number of bands than usual.
IGH-FGFR3 t(4;14) translocation
bone marrow aspirate
1.0
H00
7-10
FISH
(Various) Band Culture lymphocytes or bone marrow cells, and fix metaphase cells. This method then stains the chromosomes with a dye to create a striped pattern (band), and analyzes the distribution and density of the band. G-Banding, which performs Giemsa staining after treatment with trypsin solution, C-Banding, which performs Giemsa staining after treatment with HCI, Ba (OH) 2, 2×SCC, these include Q-Banding, which involves staining with quinacrine mustard and then observing with a fluorescence microscope, and high-precision banding, which uses mitotic images from the end of prophase to the beginning of metaphase, and observes a larger number of bands than usual.
IGH-FGFR3 t(4;14) translocation
Blood (heparin added)
5.0
PH5
7-10
FISH
(Various) Band Culture lymphocytes or bone marrow cells, and fix metaphase cells. This method then stains the chromosomes with a dye to create a striped pattern (band), and analyzes the distribution and density of the band. G-Banding, which performs Giemsa staining after treatment with trypsin solution, C-Banding, which performs Giemsa staining after treatment with HCI, Ba (OH) 2, 2×SCC, these include Q-Banding, which involves staining with quinacrine mustard and then observing with a fluorescence microscope, and high-precision banding, which uses mitotic images from the end of prophase to the beginning of metaphase, and observes a larger number of bands than usual.
FIP1L1-PDGFRA del(4) long arm deletion (4q12 deletion)
bone marrow aspirate
1.0
H00
7-10
FISH
(Various) Band Culture lymphocytes or bone marrow cells, and fix metaphase cells. This method then stains the chromosomes with a dye to create a striped pattern (band), and analyzes the distribution and density of the band. G-Banding, which performs Giemsa staining after treatment with trypsin solution, C-Banding, which performs Giemsa staining after treatment with HCI, Ba (OH) 2, 2×SCC, these include Q-Banding, which involves staining with quinacrine mustard and then observing with a fluorescence microscope, and high-precision banding, which uses mitotic images from the end of prophase to the beginning of metaphase, and observes a larger number of bands than usual.
FIP1L1-PDGFRA del(4) long arm deletion (4q12 deletion)
Blood (heparin added)
5.0
PH5
7-10
FISH
(Various) Band Culture lymphocytes or bone marrow cells, and fix metaphase cells. This method then stains the chromosomes with a dye to create a striped pattern (band), and analyzes the distribution and density of the band. G-Banding, which performs Giemsa staining after treatment with trypsin solution, C-Banding, which performs Giemsa staining after treatment with HCI, Ba (OH) 2, 2×SCC, these include Q-Banding, which involves staining with quinacrine mustard and then observing with a fluorescence microscope, and high-precision banding, which uses mitotic images from the end of prophase to the beginning of metaphase, and observes a larger number of bands than usual.
CSF1R del(5) long arm deletion
bone marrow aspirate
1.0
H00
7-10
FISH
(Various) Band Culture lymphocytes or bone marrow cells, and fix metaphase cells. This method then stains the chromosomes with a dye to create a striped pattern (band), and analyzes the distribution and density of the band. G-Banding, which performs Giemsa staining after treatment with trypsin solution, C-Banding, which performs Giemsa staining after treatment with HCI, Ba (OH) 2, 2×SCC, these include Q-Banding, which involves staining with quinacrine mustard and then observing with a fluorescence microscope, and high-precision banding, which uses mitotic images from the end of prophase to the beginning of metaphase, and observes a larger number of bands than usual.
CSF1R del(5) long arm deletion
Blood (heparin added)
5.0
PH5
7-10
FISH
(Various) Band Culture lymphocytes or bone marrow cells, and fix metaphase cells. This method then stains the chromosomes with a dye to create a striped pattern (band), and analyzes the distribution and density of the band. G-Banding, which performs Giemsa staining after treatment with trypsin solution, C-Banding, which performs Giemsa staining after treatment with HCI, Ba (OH) 2, 2×SCC, these include Q-Banding, which involves staining with quinacrine mustard and then observing with a fluorescence microscope, and high-precision banding, which uses mitotic images from the end of prophase to the beginning of metaphase, and observes a larger number of bands than usual.
EGR1 del(5) long arm deletion
bone marrow aspirate
1.0
H00
7-10
FISH
(Various) Band Culture lymphocytes or bone marrow cells, and fix metaphase cells. This method then stains the chromosomes with a dye to create a striped pattern (band), and analyzes the distribution and density of the band. G-Banding, which performs Giemsa staining after treatment with trypsin solution, C-Banding, which performs Giemsa staining after treatment with HCI, Ba (OH) 2, 2×SCC, these include Q-Banding, which involves staining with quinacrine mustard and then observing with a fluorescence microscope, and high-precision banding, which uses mitotic images from the end of prophase to the beginning of metaphase, and observes a larger number of bands than usual.
EGR1 del(5) long arm deletion
Blood (heparin added)
5.0
PH5
7-10
FISH
(Various) Band Culture lymphocytes or bone marrow cells, and fix metaphase cells. This method then stains the chromosomes with a dye to create a striped pattern (band), and analyzes the distribution and density of the band. G-Banding, which performs Giemsa staining after treatment with trypsin solution, C-Banding, which performs Giemsa staining after treatment with HCI, Ba (OH) 2, 2×SCC, these include Q-Banding, which involves staining with quinacrine mustard and then observing with a fluorescence microscope, and high-precision banding, which uses mitotic images from the end of prophase to the beginning of metaphase, and observes a larger number of bands than usual.
PDGFRB 5q32 translocation
bone marrow aspirate
1.0
H00
7-10
FISH
(Various) Band Culture lymphocytes or bone marrow cells, and fix metaphase cells. This method then stains the chromosomes with a dye to create a striped pattern (band), and analyzes the distribution and density of the band. G-Banding, which performs Giemsa staining after treatment with trypsin solution, C-Banding, which performs Giemsa staining after treatment with HCI, Ba (OH) 2, 2×SCC, these include Q-Banding, which involves staining with quinacrine mustard and then observing with a fluorescence microscope, and high-precision banding, which uses mitotic images from the end of prophase to the beginning of metaphase, and observes a larger number of bands than usual.
PDGFRB 5q32 translocation
Blood (heparin added)
5.0
PH5
7-10
FISH
(Various) Band Culture lymphocytes or bone marrow cells, and fix metaphase cells. This method then stains the chromosomes with a dye to create a striped pattern (band), and analyzes the distribution and density of the band. G-Banding, which performs Giemsa staining after treatment with trypsin solution, C-Banding, which performs Giemsa staining after treatment with HCI, Ba (OH) 2, 2×SCC, these include Q-Banding, which involves staining with quinacrine mustard and then observing with a fluorescence microscope, and high-precision banding, which uses mitotic images from the end of prophase to the beginning of metaphase, and observes a larger number of bands than usual.
D7S486 del(7) long arm deletion/chromosome 7 (monosomy 7)
bone marrow aspirate
1.0
H00
7-10
FISH
(Various) Band Culture lymphocytes or bone marrow cells, and fix metaphase cells. This method then stains the chromosomes with a dye to create a striped pattern (band), and analyzes the distribution and density of the band. G-Banding, which performs Giemsa staining after treatment with trypsin solution, C-Banding, which performs Giemsa staining after treatment with HCI, Ba (OH) 2, 2×SCC, these include Q-Banding, which involves staining with quinacrine mustard and then observing with a fluorescence microscope, and high-precision banding, which uses mitotic images from the end of prophase to the beginning of metaphase, and observes a larger number of bands than usual.
D7S486 del(7) long arm deletion/chromosome 7 (monosomy 7)
Blood (heparin added)
5.0
PH5
7-10
FISH
(Various) Band Culture lymphocytes or bone marrow cells, and fix metaphase cells. This method then stains the chromosomes with a dye to create a striped pattern (band), and analyzes the distribution and density of the band. G-Banding, which performs Giemsa staining after treatment with trypsin solution, C-Banding, which performs Giemsa staining after treatment with HCI, Ba (OH) 2, 2×SCC, these include Q-Banding, which involves staining with quinacrine mustard and then observing with a fluorescence microscope, and high-precision banding, which uses mitotic images from the end of prophase to the beginning of metaphase, and observes a larger number of bands than usual.
Chromosome 8
bone marrow aspirate
1.0
H00
7-10
FISH
(Various) Band Culture lymphocytes or bone marrow cells, and fix metaphase cells. This method then stains the chromosomes with a dye to create a striped pattern (band), and analyzes the distribution and density of the band. G-Banding, which performs Giemsa staining after treatment with trypsin solution, C-Banding, which performs Giemsa staining after treatment with HCI, Ba (OH) 2, 2×SCC, these include Q-Banding, which involves staining with quinacrine mustard and then observing with a fluorescence microscope, and high-precision banding, which uses mitotic images from the end of prophase to the beginning of metaphase, and observes a larger number of bands than usual.
Chromosome 8
Blood (heparin added)
5.0
PH5
7-10
FISH
(Various) Band Culture lymphocytes or bone marrow cells, and fix metaphase cells. This method then stains the chromosomes with a dye to create a striped pattern (band), and analyzes the distribution and density of the band. G-Banding, which performs Giemsa staining after treatment with trypsin solution, C-Banding, which performs Giemsa staining after treatment with HCI, Ba (OH) 2, 2×SCC, these include Q-Banding, which involves staining with quinacrine mustard and then observing with a fluorescence microscope, and high-precision banding, which uses mitotic images from the end of prophase to the beginning of metaphase, and observes a larger number of bands than usual.
MYC 8q24 translocation
lymph nodes
5×5×5mm
H00
7-10
FISH
(Various) Band Culture lymphocytes or bone marrow cells, and fix metaphase cells. This method then stains the chromosomes with a dye to create a striped pattern (band), and analyzes the distribution and density of the band. G-Banding, which performs Giemsa staining after treatment with trypsin solution, C-Banding, which performs Giemsa staining after treatment with HCI, Ba (OH) 2, 2×SCC, these include Q-Banding, which involves staining with quinacrine mustard and then observing with a fluorescence microscope, and high-precision banding, which uses mitotic images from the end of prophase to the beginning of metaphase, and observes a larger number of bands than usual.
MYC 8q24 translocation
bone marrow aspirate
1.0
H00
7-10
FISH
(Various) Band Culture lymphocytes or bone marrow cells, and fix metaphase cells. This method then stains the chromosomes with a dye to create a striped pattern (band), and analyzes the distribution and density of the band. G-Banding, which performs Giemsa staining after treatment with trypsin solution, C-Banding, which performs Giemsa staining after treatment with HCI, Ba (OH) 2, 2×SCC, these include Q-Banding, which involves staining with quinacrine mustard and then observing with a fluorescence microscope, and high-precision banding, which uses mitotic images from the end of prophase to the beginning of metaphase, and observes a larger number of bands than usual.
MYC 8q24 translocation
Blood (heparin added)
5.0
PH5
7-10
FISH
(Various) Band Culture lymphocytes or bone marrow cells, and fix metaphase cells. This method then stains the chromosomes with a dye to create a striped pattern (band), and analyzes the distribution and density of the band. G-Banding, which performs Giemsa staining after treatment with trypsin solution, C-Banding, which performs Giemsa staining after treatment with HCI, Ba (OH) 2, 2×SCC, these include Q-Banding, which involves staining with quinacrine mustard and then observing with a fluorescence microscope, and high-precision banding, which uses mitotic images from the end of prophase to the beginning of metaphase, and observes a larger number of bands than usual.
IGH-MYC t(8;14) translocation
lymph nodes
5×5×5mm
H00
7-10
FISH
(Various) Band Culture lymphocytes or bone marrow cells, and fix metaphase cells. This method then stains the chromosomes with a dye to create a striped pattern (band), and analyzes the distribution and density of the band. G-Banding, which performs Giemsa staining after treatment with trypsin solution, C-Banding, which performs Giemsa staining after treatment with HCI, Ba (OH) 2, 2×SCC, these include Q-Banding, which involves staining with quinacrine mustard and then observing with a fluorescence microscope, and high-precision banding, which uses mitotic images from the end of prophase to the beginning of metaphase, and observes a larger number of bands than usual.
IGH-MYC t(8;14) translocation
bone marrow aspirate
1.0
H00
7-10
FISH
(Various) Band Culture lymphocytes or bone marrow cells, and fix metaphase cells. This method then stains the chromosomes with a dye to create a striped pattern (band), and analyzes the distribution and density of the band. G-Banding, which performs Giemsa staining after treatment with trypsin solution, C-Banding, which performs Giemsa staining after treatment with HCI, Ba (OH) 2, 2×SCC, these include Q-Banding, which involves staining with quinacrine mustard and then observing with a fluorescence microscope, and high-precision banding, which uses mitotic images from the end of prophase to the beginning of metaphase, and observes a larger number of bands than usual.
IGH-MYC t(8;14) translocation
Blood (heparin added)
5.0
PH5
7-10
FISH
(Various) Band Culture lymphocytes or bone marrow cells, and fix metaphase cells. This method then stains the chromosomes with a dye to create a striped pattern (band), and analyzes the distribution and density of the band. G-Banding, which performs Giemsa staining after treatment with trypsin solution, C-Banding, which performs Giemsa staining after treatment with HCI, Ba (OH) 2, 2×SCC, these include Q-Banding, which involves staining with quinacrine mustard and then observing with a fluorescence microscope, and high-precision banding, which uses mitotic images from the end of prophase to the beginning of metaphase, and observes a larger number of bands than usual.
RUNX1-RUNX1T1(AML1-MTG8) t(8;21) translocation
bone marrow aspirate
1.0
H00
7-10
FISH
(Various) Band Culture lymphocytes or bone marrow cells, and fix metaphase cells. This method then stains the chromosomes with a dye to create a striped pattern (band), and analyzes the distribution and density of the band. G-Banding, which performs Giemsa staining after treatment with trypsin solution, C-Banding, which performs Giemsa staining after treatment with HCI, Ba (OH) 2, 2×SCC, these include Q-Banding, which involves staining with quinacrine mustard and then observing with a fluorescence microscope, and high-precision banding, which uses mitotic images from the end of prophase to the beginning of metaphase, and observes a larger number of bands than usual.
RUNX1-RUNX1T1(AML1-MTG8) t(8;21) translocation
Blood (heparin added)
5.0
PH5
7-10
FISH
(Various) Band Culture lymphocytes or bone marrow cells, and fix metaphase cells. This method then stains the chromosomes with a dye to create a striped pattern (band), and analyzes the distribution and density of the band. G-Banding, which performs Giemsa staining after treatment with trypsin solution, C-Banding, which performs Giemsa staining after treatment with HCI, Ba (OH) 2, 2×SCC, these include Q-Banding, which involves staining with quinacrine mustard and then observing with a fluorescence microscope, and high-precision banding, which uses mitotic images from the end of prophase to the beginning of metaphase, and observes a larger number of bands than usual.
FGFR1 8p11.2 translocation
bone marrow aspirate
1.0
H00
7-10
FISH
(Various) Band Culture lymphocytes or bone marrow cells, and fix metaphase cells. This method then stains the chromosomes with a dye to create a striped pattern (band), and analyzes the distribution and density of the band. G-Banding, which performs Giemsa staining after treatment with trypsin solution, C-Banding, which performs Giemsa staining after treatment with HCI, Ba (OH) 2, 2×SCC, these include Q-Banding, which involves staining with quinacrine mustard and then observing with a fluorescence microscope, and high-precision banding, which uses mitotic images from the end of prophase to the beginning of metaphase, and observes a larger number of bands than usual.
FGFR1 8p11.2 translocation
Blood (heparin added)
5.0
PH5
7-10
FISH
(Various) Band Culture lymphocytes or bone marrow cells, and fix metaphase cells. This method then stains the chromosomes with a dye to create a striped pattern (band), and analyzes the distribution and density of the band. G-Banding, which performs Giemsa staining after treatment with trypsin solution, C-Banding, which performs Giemsa staining after treatment with HCI, Ba (OH) 2, 2×SCC, these include Q-Banding, which involves staining with quinacrine mustard and then observing with a fluorescence microscope, and high-precision banding, which uses mitotic images from the end of prophase to the beginning of metaphase, and observes a larger number of bands than usual.
BCR-ABL1 t(9;22) translocation
bone marrow aspirate
1.0
H00
7-10
FISH
(Various) Band Culture lymphocytes or bone marrow cells, and fix metaphase cells. This method then stains the chromosomes with a dye to create a striped pattern (band), and analyzes the distribution and density of the band. G-Banding, which performs Giemsa staining after treatment with trypsin solution, C-Banding, which performs Giemsa staining after treatment with HCI, Ba (OH) 2, 2×SCC, these include Q-Banding, which involves staining with quinacrine mustard and then observing with a fluorescence microscope, and high-precision banding, which uses mitotic images from the end of prophase to the beginning of metaphase, and observes a larger number of bands than usual.
BCR-ABL1 t(9;22) translocation
Blood (heparin added)
5.0
PH5
7-10
FISH
(Various) Band Culture lymphocytes or bone marrow cells, and fix metaphase cells. This method then stains the chromosomes with a dye to create a striped pattern (band), and analyzes the distribution and density of the band. G-Banding, which performs Giemsa staining after treatment with trypsin solution, C-Banding, which performs Giemsa staining after treatment with HCI, Ba (OH) 2, 2×SCC, these include Q-Banding, which involves staining with quinacrine mustard and then observing with a fluorescence microscope, and high-precision banding, which uses mitotic images from the end of prophase to the beginning of metaphase, and observes a larger number of bands than usual.
(Various) Band Culture lymphocytes or bone marrow cells, and fix metaphase cells. This method then stains the chromosomes with a dye to create a striped pattern (band), and analyzes the distribution and density of the band. G-Banding, which performs Giemsa staining after treatment with trypsin solution, C-Banding, which performs Giemsa staining after treatment with HCI, Ba (OH) 2, 2×SCC, these include Q-Banding, which involves staining with quinacrine mustard and then observing with a fluorescence microscope, and high-precision banding, which uses mitotic images from the end of prophase to the beginning of metaphase, and observes a larger number of bands than usual.
KMT2A(MLL) 11q23.3 translocation
bone marrow aspirate
1.0
H00
7-10
FISH
(Various) Band Culture lymphocytes or bone marrow cells, and fix metaphase cells. This method then stains the chromosomes with a dye to create a striped pattern (band), and analyzes the distribution and density of the band. G-Banding, which performs Giemsa staining after treatment with trypsin solution, C-Banding, which performs Giemsa staining after treatment with HCI, Ba (OH) 2, 2×SCC, these include Q-Banding, which involves staining with quinacrine mustard and then observing with a fluorescence microscope, and high-precision banding, which uses mitotic images from the end of prophase to the beginning of metaphase, and observes a larger number of bands than usual.
KMT2A(MLL) 11q23.3 translocation
Blood (heparin added)
5.0
PH5
7-10
FISH
(Various) Band Culture lymphocytes or bone marrow cells, and fix metaphase cells. This method then stains the chromosomes with a dye to create a striped pattern (band), and analyzes the distribution and density of the band. G-Banding, which performs Giemsa staining after treatment with trypsin solution, C-Banding, which performs Giemsa staining after treatment with HCI, Ba (OH) 2, 2×SCC, these include Q-Banding, which involves staining with quinacrine mustard and then observing with a fluorescence microscope, and high-precision banding, which uses mitotic images from the end of prophase to the beginning of metaphase, and observes a larger number of bands than usual.
IGH-CCND1(IGH-BCL1) t(11;14) translocation
lymph nodes
5×5×5mm
H00
7-10
FISH
(Various) Band Culture lymphocytes or bone marrow cells, and fix metaphase cells. This method then stains the chromosomes with a dye to create a striped pattern (band), and analyzes the distribution and density of the band. G-Banding, which performs Giemsa staining after treatment with trypsin solution, C-Banding, which performs Giemsa staining after treatment with HCI, Ba (OH) 2, 2×SCC, these include Q-Banding, which involves staining with quinacrine mustard and then observing with a fluorescence microscope, and high-precision banding, which uses mitotic images from the end of prophase to the beginning of metaphase, and observes a larger number of bands than usual.
IGH-CCND1(IGH-BCL1) t(11;14) translocation
bone marrow aspirate
1.0
H00
7-10
FISH
(Various) Band Culture lymphocytes or bone marrow cells, and fix metaphase cells. This method then stains the chromosomes with a dye to create a striped pattern (band), and analyzes the distribution and density of the band. G-Banding, which performs Giemsa staining after treatment with trypsin solution, C-Banding, which performs Giemsa staining after treatment with HCI, Ba (OH) 2, 2×SCC, these include Q-Banding, which involves staining with quinacrine mustard and then observing with a fluorescence microscope, and high-precision banding, which uses mitotic images from the end of prophase to the beginning of metaphase, and observes a larger number of bands than usual.
IGH-CCND1(IGH-BCL1) t(11;14) translocation
Blood (heparin added)
5.0
PH5
7-10
FISH
(Various) Band Culture lymphocytes or bone marrow cells, and fix metaphase cells. This method then stains the chromosomes with a dye to create a striped pattern (band), and analyzes the distribution and density of the band. G-Banding, which performs Giemsa staining after treatment with trypsin solution, C-Banding, which performs Giemsa staining after treatment with HCI, Ba (OH) 2, 2×SCC, these include Q-Banding, which involves staining with quinacrine mustard and then observing with a fluorescence microscope, and high-precision banding, which uses mitotic images from the end of prophase to the beginning of metaphase, and observes a larger number of bands than usual.
NUP98 11p15 translocation
bone marrow aspirate
1.0
H00
7-10
FISH
(Various) Band Culture lymphocytes or bone marrow cells, and fix metaphase cells. This method then stains the chromosomes with a dye to create a striped pattern (band), and analyzes the distribution and density of the band. G-Banding, which performs Giemsa staining after treatment with trypsin solution, C-Banding, which performs Giemsa staining after treatment with HCI, Ba (OH) 2, 2×SCC, these include Q-Banding, which involves staining with quinacrine mustard and then observing with a fluorescence microscope, and high-precision banding, which uses mitotic images from the end of prophase to the beginning of metaphase, and observes a larger number of bands than usual.
NUP98 11p15 translocation
Blood (heparin added)
5.0
PH5
7-10
FISH
(Various) Band Culture lymphocytes or bone marrow cells, and fix metaphase cells. This method then stains the chromosomes with a dye to create a striped pattern (band), and analyzes the distribution and density of the band. G-Banding, which performs Giemsa staining after treatment with trypsin solution, C-Banding, which performs Giemsa staining after treatment with HCI, Ba (OH) 2, 2×SCC, these include Q-Banding, which involves staining with quinacrine mustard and then observing with a fluorescence microscope, and high-precision banding, which uses mitotic images from the end of prophase to the beginning of metaphase, and observes a larger number of bands than usual.
BIRC3-MALT1(API2-MALT1) t(11;18) translocation
lymph nodes
5×5×5mm
H00
7-10
FISH
(Various) Band Culture lymphocytes or bone marrow cells, and fix metaphase cells. This method then stains the chromosomes with a dye to create a striped pattern (band), and analyzes the distribution and density of the band. G-Banding, which performs Giemsa staining after treatment with trypsin solution, C-Banding, which performs Giemsa staining after treatment with HCI, Ba (OH) 2, 2×SCC, these include Q-Banding, which involves staining with quinacrine mustard and then observing with a fluorescence microscope, and high-precision banding, which uses mitotic images from the end of prophase to the beginning of metaphase, and observes a larger number of bands than usual.
BIRC3-MALT1(API2-MALT1) t(11;18) translocation
bone marrow aspirate
1.0
H00
7-10
FISH
(Various) Band Culture lymphocytes or bone marrow cells, and fix metaphase cells. This method then stains the chromosomes with a dye to create a striped pattern (band), and analyzes the distribution and density of the band. G-Banding, which performs Giemsa staining after treatment with trypsin solution, C-Banding, which performs Giemsa staining after treatment with HCI, Ba (OH) 2, 2×SCC, these include Q-Banding, which involves staining with quinacrine mustard and then observing with a fluorescence microscope, and high-precision banding, which uses mitotic images from the end of prophase to the beginning of metaphase, and observes a larger number of bands than usual.
BIRC3-MALT1(API2-MALT1) t(11;18) translocation
Blood (heparin added)
5.0
PH5
7-10
FISH
(Various) Band Culture lymphocytes or bone marrow cells, and fix metaphase cells. This method then stains the chromosomes with a dye to create a striped pattern (band), and analyzes the distribution and density of the band. G-Banding, which performs Giemsa staining after treatment with trypsin solution, C-Banding, which performs Giemsa staining after treatment with HCI, Ba (OH) 2, 2×SCC, these include Q-Banding, which involves staining with quinacrine mustard and then observing with a fluorescence microscope, and high-precision banding, which uses mitotic images from the end of prophase to the beginning of metaphase, and observes a larger number of bands than usual.
ATM del(11) long arm deletion
bone marrow aspirate
1.0
H00
7-10
FISH
(Various) Band Culture lymphocytes or bone marrow cells, and fix metaphase cells. This method then stains the chromosomes with a dye to create a striped pattern (band), and analyzes the distribution and density of the band. G-Banding, which performs Giemsa staining after treatment with trypsin solution, C-Banding, which performs Giemsa staining after treatment with HCI, Ba (OH) 2, 2×SCC, these include Q-Banding, which involves staining with quinacrine mustard and then observing with a fluorescence microscope, and high-precision banding, which uses mitotic images from the end of prophase to the beginning of metaphase, and observes a larger number of bands than usual.
ATM del(11) long arm deletion
Blood (heparin added)
5.0
PH5
7-10
FISH
(Various) Band Culture lymphocytes or bone marrow cells, and fix metaphase cells. This method then stains the chromosomes with a dye to create a striped pattern (band), and analyzes the distribution and density of the band. G-Banding, which performs Giemsa staining after treatment with trypsin solution, C-Banding, which performs Giemsa staining after treatment with HCI, Ba (OH) 2, 2×SCC, these include Q-Banding, which involves staining with quinacrine mustard and then observing with a fluorescence microscope, and high-precision banding, which uses mitotic images from the end of prophase to the beginning of metaphase, and observes a larger number of bands than usual.
Chromosome 12
bone marrow aspirate
1.0
H00
7-10
FISH
(Various) Band Culture lymphocytes or bone marrow cells, and fix metaphase cells. This method then stains the chromosomes with a dye to create a striped pattern (band), and analyzes the distribution and density of the band. G-Banding, which performs Giemsa staining after treatment with trypsin solution, C-Banding, which performs Giemsa staining after treatment with HCI, Ba (OH) 2, 2×SCC, these include Q-Banding, which involves staining with quinacrine mustard and then observing with a fluorescence microscope, and high-precision banding, which uses mitotic images from the end of prophase to the beginning of metaphase, and observes a larger number of bands than usual.
Chromosome 12
Blood (heparin added)
5.0
PH5
7-10
FISH
(Various) Band Culture lymphocytes or bone marrow cells, and fix metaphase cells. This method then stains the chromosomes with a dye to create a striped pattern (band), and analyzes the distribution and density of the band. G-Banding, which performs Giemsa staining after treatment with trypsin solution, C-Banding, which performs Giemsa staining after treatment with HCI, Ba (OH) 2, 2×SCC, these include Q-Banding, which involves staining with quinacrine mustard and then observing with a fluorescence microscope, and high-precision banding, which uses mitotic images from the end of prophase to the beginning of metaphase, and observes a larger number of bands than usual.
ETV6-RUNX1(TEL-AML1) t(12;21) translocation
bone marrow aspirate
1.0
H00
7-10
FISH
(Various) Band Culture lymphocytes or bone marrow cells, and fix metaphase cells. This method then stains the chromosomes with a dye to create a striped pattern (band), and analyzes the distribution and density of the band. G-Banding, which performs Giemsa staining after treatment with trypsin solution, C-Banding, which performs Giemsa staining after treatment with HCI, Ba (OH) 2, 2×SCC, these include Q-Banding, which involves staining with quinacrine mustard and then observing with a fluorescence microscope, and high-precision banding, which uses mitotic images from the end of prophase to the beginning of metaphase, and observes a larger number of bands than usual.
ETV6-RUNX1(TEL-AML1) t(12;21) translocation
Blood (heparin added)
5.0
PH5
7-10
FISH
(Various) Band Culture lymphocytes or bone marrow cells, and fix metaphase cells. This method then stains the chromosomes with a dye to create a striped pattern (band), and analyzes the distribution and density of the band. G-Banding, which performs Giemsa staining after treatment with trypsin solution, C-Banding, which performs Giemsa staining after treatment with HCI, Ba (OH) 2, 2×SCC, these include Q-Banding, which involves staining with quinacrine mustard and then observing with a fluorescence microscope, and high-precision banding, which uses mitotic images from the end of prophase to the beginning of metaphase, and observes a larger number of bands than usual.
D13S319 del(13) long arm deletion
bone marrow aspirate
1.0
H00
7-10
FISH
(Various) Band Culture lymphocytes or bone marrow cells, and fix metaphase cells. This method then stains the chromosomes with a dye to create a striped pattern (band), and analyzes the distribution and density of the band. G-Banding, which performs Giemsa staining after treatment with trypsin solution, C-Banding, which performs Giemsa staining after treatment with HCI, Ba (OH) 2, 2×SCC, these include Q-Banding, which involves staining with quinacrine mustard and then observing with a fluorescence microscope, and high-precision banding, which uses mitotic images from the end of prophase to the beginning of metaphase, and observes a larger number of bands than usual.
D13S319 del(13) long arm deletion
Blood (heparin added)
5.0
PH5
7-10
FISH
(Various) Band Culture lymphocytes or bone marrow cells, and fix metaphase cells. This method then stains the chromosomes with a dye to create a striped pattern (band), and analyzes the distribution and density of the band. G-Banding, which performs Giemsa staining after treatment with trypsin solution, C-Banding, which performs Giemsa staining after treatment with HCI, Ba (OH) 2, 2×SCC, these include Q-Banding, which involves staining with quinacrine mustard and then observing with a fluorescence microscope, and high-precision banding, which uses mitotic images from the end of prophase to the beginning of metaphase, and observes a larger number of bands than usual.
IGH-BCL2 t(14;18) translocation
lymph nodes
5×5×5mm
H00
7-10
FISH
(Various) Band Culture lymphocytes or bone marrow cells, and fix metaphase cells. This method then stains the chromosomes with a dye to create a striped pattern (band), and analyzes the distribution and density of the band. G-Banding, which performs Giemsa staining after treatment with trypsin solution, C-Banding, which performs Giemsa staining after treatment with HCI, Ba (OH) 2, 2×SCC, these include Q-Banding, which involves staining with quinacrine mustard and then observing with a fluorescence microscope, and high-precision banding, which uses mitotic images from the end of prophase to the beginning of metaphase, and observes a larger number of bands than usual.
IGH-BCL2 t(14;18) translocation
bone marrow aspirate
1.0
H00
7-10
FISH
(Various) Band Culture lymphocytes or bone marrow cells, and fix metaphase cells. This method then stains the chromosomes with a dye to create a striped pattern (band), and analyzes the distribution and density of the band. G-Banding, which performs Giemsa staining after treatment with trypsin solution, C-Banding, which performs Giemsa staining after treatment with HCI, Ba (OH) 2, 2×SCC, these include Q-Banding, which involves staining with quinacrine mustard and then observing with a fluorescence microscope, and high-precision banding, which uses mitotic images from the end of prophase to the beginning of metaphase, and observes a larger number of bands than usual.
IGH-BCL2 t(14;18) translocation
Blood (heparin added)
5.0
PH5
7-10
FISH
(Various) Band Culture lymphocytes or bone marrow cells, and fix metaphase cells. This method then stains the chromosomes with a dye to create a striped pattern (band), and analyzes the distribution and density of the band. G-Banding, which performs Giemsa staining after treatment with trypsin solution, C-Banding, which performs Giemsa staining after treatment with HCI, Ba (OH) 2, 2×SCC, these include Q-Banding, which involves staining with quinacrine mustard and then observing with a fluorescence microscope, and high-precision banding, which uses mitotic images from the end of prophase to the beginning of metaphase, and observes a larger number of bands than usual.
IGH-MAF t(14;16) translocation
bone marrow aspirate
1.0
H00
7-10
FISH
(Various) Band Culture lymphocytes or bone marrow cells, and fix metaphase cells. This method then stains the chromosomes with a dye to create a striped pattern (band), and analyzes the distribution and density of the band. G-Banding, which performs Giemsa staining after treatment with trypsin solution, C-Banding, which performs Giemsa staining after treatment with HCI, Ba (OH) 2, 2×SCC, these include Q-Banding, which involves staining with quinacrine mustard and then observing with a fluorescence microscope, and high-precision banding, which uses mitotic images from the end of prophase to the beginning of metaphase, and observes a larger number of bands than usual.
IGH-MAF t(14;16) translocation
Blood (heparin added)
5.0
PH5
7-10
FISH
(Various) Band Culture lymphocytes or bone marrow cells, and fix metaphase cells. This method then stains the chromosomes with a dye to create a striped pattern (band), and analyzes the distribution and density of the band. G-Banding, which performs Giemsa staining after treatment with trypsin solution, C-Banding, which performs Giemsa staining after treatment with HCI, Ba (OH) 2, 2×SCC, these include Q-Banding, which involves staining with quinacrine mustard and then observing with a fluorescence microscope, and high-precision banding, which uses mitotic images from the end of prophase to the beginning of metaphase, and observes a larger number of bands than usual.
PML-RARA t(15;17) translocation
bone marrow aspirate
1.0
H00
6-9
FISH
(Various) Band Culture lymphocytes or bone marrow cells, and fix metaphase cells. This method then stains the chromosomes with a dye to create a striped pattern (band), and analyzes the distribution and density of the band. G-Banding, which performs Giemsa staining after treatment with trypsin solution, C-Banding, which performs Giemsa staining after treatment with HCI, Ba (OH) 2, 2×SCC, these include Q-Banding, which involves staining with quinacrine mustard and then observing with a fluorescence microscope, and high-precision banding, which uses mitotic images from the end of prophase to the beginning of metaphase, and observes a larger number of bands than usual.
PML-RARA t(15;17) translocation
Blood (heparin added)
5.0
PH5
6-9
FISH
(Various) Band Culture lymphocytes or bone marrow cells, and fix metaphase cells. This method then stains the chromosomes with a dye to create a striped pattern (band), and analyzes the distribution and density of the band. G-Banding, which performs Giemsa staining after treatment with trypsin solution, C-Banding, which performs Giemsa staining after treatment with HCI, Ba (OH) 2, 2×SCC, these include Q-Banding, which involves staining with quinacrine mustard and then observing with a fluorescence microscope, and high-precision banding, which uses mitotic images from the end of prophase to the beginning of metaphase, and observes a larger number of bands than usual.
CBFB inv(16) inversion, t(16;16) translocation
bone marrow aspirate
1.0
H00
7-10
FISH
(Various) Band Culture lymphocytes or bone marrow cells, and fix metaphase cells. This method then stains the chromosomes with a dye to create a striped pattern (band), and analyzes the distribution and density of the band. G-Banding, which performs Giemsa staining after treatment with trypsin solution, C-Banding, which performs Giemsa staining after treatment with HCI, Ba (OH) 2, 2×SCC, these include Q-Banding, which involves staining with quinacrine mustard and then observing with a fluorescence microscope, and high-precision banding, which uses mitotic images from the end of prophase to the beginning of metaphase, and observes a larger number of bands than usual.
CBFB inv(16) inversion, t(16;16) translocation
Blood (heparin added)
5.0
PH5
7-10
FISH
(Various) Band Culture lymphocytes or bone marrow cells, and fix metaphase cells. This method then stains the chromosomes with a dye to create a striped pattern (band), and analyzes the distribution and density of the band. G-Banding, which performs Giemsa staining after treatment with trypsin solution, C-Banding, which performs Giemsa staining after treatment with HCI, Ba (OH) 2, 2×SCC, these include Q-Banding, which involves staining with quinacrine mustard and then observing with a fluorescence microscope, and high-precision banding, which uses mitotic images from the end of prophase to the beginning of metaphase, and observes a larger number of bands than usual.
TP53 del(17) short arm missing
bone marrow aspirate
1.0
H00
7-10
FISH
(Various) Band Culture lymphocytes or bone marrow cells, and fix metaphase cells. This method then stains the chromosomes with a dye to create a striped pattern (band), and analyzes the distribution and density of the band. G-Banding, which performs Giemsa staining after treatment with trypsin solution, C-Banding, which performs Giemsa staining after treatment with HCI, Ba (OH) 2, 2×SCC, these include Q-Banding, which involves staining with quinacrine mustard and then observing with a fluorescence microscope, and high-precision banding, which uses mitotic images from the end of prophase to the beginning of metaphase, and observes a larger number of bands than usual.
TP53 del(17) short arm missing
Blood (heparin added)
5.0
PH5
7-10
FISH
(Various) Band Culture lymphocytes or bone marrow cells, and fix metaphase cells. This method then stains the chromosomes with a dye to create a striped pattern (band), and analyzes the distribution and density of the band. G-Banding, which performs Giemsa staining after treatment with trypsin solution, C-Banding, which performs Giemsa staining after treatment with HCI, Ba (OH) 2, 2×SCC, these include Q-Banding, which involves staining with quinacrine mustard and then observing with a fluorescence microscope, and high-precision banding, which uses mitotic images from the end of prophase to the beginning of metaphase, and observes a larger number of bands than usual.
MALT1 18q21 translocation
lymph nodes
5×5×5mm
H00
7-10
FISH
(Various) Band Culture lymphocytes or bone marrow cells, and fix metaphase cells. This method then stains the chromosomes with a dye to create a striped pattern (band), and analyzes the distribution and density of the band. G-Banding, which performs Giemsa staining after treatment with trypsin solution, C-Banding, which performs Giemsa staining after treatment with HCI, Ba (OH) 2, 2×SCC, these include Q-Banding, which involves staining with quinacrine mustard and then observing with a fluorescence microscope, and high-precision banding, which uses mitotic images from the end of prophase to the beginning of metaphase, and observes a larger number of bands than usual.
MALT1 18q21 translocation
bone marrow aspirate
1.0
H00
7-10
FISH
(Various) Band Culture lymphocytes or bone marrow cells, and fix metaphase cells. This method then stains the chromosomes with a dye to create a striped pattern (band), and analyzes the distribution and density of the band. G-Banding, which performs Giemsa staining after treatment with trypsin solution, C-Banding, which performs Giemsa staining after treatment with HCI, Ba (OH) 2, 2×SCC, these include Q-Banding, which involves staining with quinacrine mustard and then observing with a fluorescence microscope, and high-precision banding, which uses mitotic images from the end of prophase to the beginning of metaphase, and observes a larger number of bands than usual.
MALT1 18q21 translocation
Blood (heparin added)
5.0
PH5
7-10
FISH
(Various) Band Culture lymphocytes or bone marrow cells, and fix metaphase cells. This method then stains the chromosomes with a dye to create a striped pattern (band), and analyzes the distribution and density of the band. G-Banding, which performs Giemsa staining after treatment with trypsin solution, C-Banding, which performs Giemsa staining after treatment with HCI, Ba (OH) 2, 2×SCC, these include Q-Banding, which involves staining with quinacrine mustard and then observing with a fluorescence microscope, and high-precision banding, which uses mitotic images from the end of prophase to the beginning of metaphase, and observes a larger number of bands than usual.
BCL2 18q21 translocation
lymph nodes
5×5×5mm
H00
7-10
FISH
(Various) Band Culture lymphocytes or bone marrow cells, and fix metaphase cells. This method then stains the chromosomes with a dye to create a striped pattern (band), and analyzes the distribution and density of the band. G-Banding, which performs Giemsa staining after treatment with trypsin solution, C-Banding, which performs Giemsa staining after treatment with HCI, Ba (OH) 2, 2×SCC, these include Q-Banding, which involves staining with quinacrine mustard and then observing with a fluorescence microscope, and high-precision banding, which uses mitotic images from the end of prophase to the beginning of metaphase, and observes a larger number of bands than usual.
BCL2 18q21 translocation
bone marrow aspirate
1.0
H00
7-10
FISH
(Various) Band Culture lymphocytes or bone marrow cells, and fix metaphase cells. This method then stains the chromosomes with a dye to create a striped pattern (band), and analyzes the distribution and density of the band. G-Banding, which performs Giemsa staining after treatment with trypsin solution, C-Banding, which performs Giemsa staining after treatment with HCI, Ba (OH) 2, 2×SCC, these include Q-Banding, which involves staining with quinacrine mustard and then observing with a fluorescence microscope, and high-precision banding, which uses mitotic images from the end of prophase to the beginning of metaphase, and observes a larger number of bands than usual.
BCL2 18q21 translocation
Blood (heparin added)
5.0
PH5
7-10
FISH
(Various) Band Culture lymphocytes or bone marrow cells, and fix metaphase cells. This method then stains the chromosomes with a dye to create a striped pattern (band), and analyzes the distribution and density of the band. G-Banding, which performs Giemsa staining after treatment with trypsin solution, C-Banding, which performs Giemsa staining after treatment with HCI, Ba (OH) 2, 2×SCC, these include Q-Banding, which involves staining with quinacrine mustard and then observing with a fluorescence microscope, and high-precision banding, which uses mitotic images from the end of prophase to the beginning of metaphase, and observes a larger number of bands than usual.
del(20) long arm missing
bone marrow aspirate
1.0
H00
7-10
FISH
(Various) Band Culture lymphocytes or bone marrow cells, and fix metaphase cells. This method then stains the chromosomes with a dye to create a striped pattern (band), and analyzes the distribution and density of the band. G-Banding, which performs Giemsa staining after treatment with trypsin solution, C-Banding, which performs Giemsa staining after treatment with HCI, Ba (OH) 2, 2×SCC, these include Q-Banding, which involves staining with quinacrine mustard and then observing with a fluorescence microscope, and high-precision banding, which uses mitotic images from the end of prophase to the beginning of metaphase, and observes a larger number of bands than usual.
del(20) long arm missing
Blood (heparin added)
5.0
PH5
7-10
FISH
(Various) Band Culture lymphocytes or bone marrow cells, and fix metaphase cells. This method then stains the chromosomes with a dye to create a striped pattern (band), and analyzes the distribution and density of the band. G-Banding, which performs Giemsa staining after treatment with trypsin solution, C-Banding, which performs Giemsa staining after treatment with HCI, Ba (OH) 2, 2×SCC, these include Q-Banding, which involves staining with quinacrine mustard and then observing with a fluorescence microscope, and high-precision banding, which uses mitotic images from the end of prophase to the beginning of metaphase, and observes a larger number of bands than usual.
Chromosome X
bone marrow aspirate
1.0
H00
7-10
FISH
(Various) Band Culture lymphocytes or bone marrow cells, and fix metaphase cells. This method then stains the chromosomes with a dye to create a striped pattern (band), and analyzes the distribution and density of the band. G-Banding, which performs Giemsa staining after treatment with trypsin solution, C-Banding, which performs Giemsa staining after treatment with HCI, Ba (OH) 2, 2×SCC, these include Q-Banding, which involves staining with quinacrine mustard and then observing with a fluorescence microscope, and high-precision banding, which uses mitotic images from the end of prophase to the beginning of metaphase, and observes a larger number of bands than usual.
Chromosome X
Blood (heparin added)
5.0
PH5
7-10
FISH
(Various) Band Culture lymphocytes or bone marrow cells, and fix metaphase cells. This method then stains the chromosomes with a dye to create a striped pattern (band), and analyzes the distribution and density of the band. G-Banding, which performs Giemsa staining after treatment with trypsin solution, C-Banding, which performs Giemsa staining after treatment with HCI, Ba (OH) 2, 2×SCC, these include Q-Banding, which involves staining with quinacrine mustard and then observing with a fluorescence microscope, and high-precision banding, which uses mitotic images from the end of prophase to the beginning of metaphase, and observes a larger number of bands than usual.
Chromosome Y
bone marrow aspirate
1.0
H00
7-10
FISH
(Various) Band Culture lymphocytes or bone marrow cells, and fix metaphase cells. This method then stains the chromosomes with a dye to create a striped pattern (band), and analyzes the distribution and density of the band. G-Banding, which performs Giemsa staining after treatment with trypsin solution, C-Banding, which performs Giemsa staining after treatment with HCI, Ba (OH) 2, 2×SCC, these include Q-Banding, which involves staining with quinacrine mustard and then observing with a fluorescence microscope, and high-precision banding, which uses mitotic images from the end of prophase to the beginning of metaphase, and observes a larger number of bands than usual.
Chromosome Y
Blood (heparin added)
5.0
PH5
7-10
FISH
(Various) Band Culture lymphocytes or bone marrow cells, and fix metaphase cells. This method then stains the chromosomes with a dye to create a striped pattern (band), and analyzes the distribution and density of the band. G-Banding, which performs Giemsa staining after treatment with trypsin solution, C-Banding, which performs Giemsa staining after treatment with HCI, Ba (OH) 2, 2×SCC, these include Q-Banding, which involves staining with quinacrine mustard and then observing with a fluorescence microscope, and high-precision banding, which uses mitotic images from the end of prophase to the beginning of metaphase, and observes a larger number of bands than usual.
Heterosexual BMT (bone marrow transplant) (X, Y chromosomes)
bone marrow aspirate
1.0
H00
6-10
FISH
(Various) Band Culture lymphocytes or bone marrow cells, and fix metaphase cells. This method then stains the chromosomes with a dye to create a striped pattern (band), and analyzes the distribution and density of the band. G-Banding, which performs Giemsa staining after treatment with trypsin solution, C-Banding, which performs Giemsa staining after treatment with HCI, Ba (OH) 2, 2×SCC, these include Q-Banding, which involves staining with quinacrine mustard and then observing with a fluorescence microscope, and high-precision banding, which uses mitotic images from the end of prophase to the beginning of metaphase, and observes a larger number of bands than usual.
Heterosexual BMT (bone marrow transplant) (X, Y chromosomes)
Blood (heparin added)
5.0
PH5
6-10
FISH
(Various) Band Culture lymphocytes or bone marrow cells, and fix metaphase cells. This method then stains the chromosomes with a dye to create a striped pattern (band), and analyzes the distribution and density of the band. G-Banding, which performs Giemsa staining after treatment with trypsin solution, C-Banding, which performs Giemsa staining after treatment with HCI, Ba (OH) 2, 2×SCC, these include Q-Banding, which involves staining with quinacrine mustard and then observing with a fluorescence microscope, and high-precision banding, which uses mitotic images from the end of prophase to the beginning of metaphase, and observes a larger number of bands than usual.
Notifications of URL changes/lab information added
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Notifications of URL changes/lab information added
You can now view test items from all labs.
Please choose a lab from the list below.
You can switch between labs as any time using the upper right lab icon.
The domain name of the TEST DIRECTORYpage has changed.
Please update bookmarks and saved links with the new address.