See Compliance Statement A: www.aruplab.com/CS
||Fluorescence in situ hybridization (FISH) panel is performed on CD138+ sorted cells (assuming specimen is sufficient for sorting) for multiple myeloma prognosis-specific genomic abnormalities: CKS1B (1q gain), ASS1 (+9), CCND1/IGH (IGH/CCND1 fusion or +11), IGH rearrangement, PML (+15) and p53 (17p deletion). If IGH is positive and not partnered with CCND1, additional testing will include FGFR3/IGH and MAF/IGH. Additional charges will apply.
This test must be ordered using Cytogenetic test request form 43097 or through your ARUP interface. Please submit the Patient History for Cytogenetics (Chromosome) Studies form with the electronic packing list. The form is available on ARUP's Web site, aruplab.com/Testing-Information/consentforms-patienthistory.jsp
A processing fee will be charged if this procedure is canceled at the client's request, after the test has been set up, or if the specimen integrity is inadequate to allow a complete analysis.
||88271 x6; 88275 x6; 88291
||Chromosome Analysis (Multiple Myeloma Panel by FISH)