I learned that I am IGHV mutated / TP53 unmutated, then received the following additional results without much commentary. Is anybody able to help interpret them?
- Chromosome Microarray Analysis (CMA) was performed on this bone marrow sample using 8x60K oligonucleotide arrays (Agilent) to screen for genome imbalances associated with CLL as only limited FISH testing was possible in this sample.
- A male genome was identified harbouring 9Mb loss at 13q14.11q14.3 regions (housing the RB1, DLEU1, DLEU2 & DLEU 7 genes among others.) indicative for standard risk CLL.
- In addition, FISH analysis of 100 cells using dual color/dual probe (Cytocell) confirmed the CMA data by showing a normal diploid signal pattern for the ATM and TP53 gene regions