CYALL (Non-Blood Sample): Fluorescence in situ hybridization (FISH) is performed to detect from non-blood samples the followings: abnormal copy numbers of chromosome 4, abnormal copy numbers of chromosome 10, abnormal copy numbers of chromosome 17/deletion of chromosome 17p13.1 (TP53), ETV6/RUNX1 gene fusion, BCR/ABL1 gene fusion, MLL rearrangements, PDGFRB rearrangements, ABL1 rearrangements, and ABL2 rearrangements.
BCYAML (Blood Sample): Fluorescence in situ hybridization (FISH) is performed to detect from blood samples the followings: abnormal copy numbers of chromosome 4, abnormal copy numbers of chromosome 10, deletion of chromosome 17p13.1 (TP53), ETV6/RUNX1 gene fusion, BCR/ABL1 gene fusion, MLL rearrangements, PDGFRB rearrangements, ABL1 rearrangements, and ABL2 rearrangements.
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