Approximately 40-60% of Multiple Myeloma cases are associated with translocations involving the IgH locus at chromosome 14q32 and one of several partners including CCND1, WHSC1 (MMSET), CCND3, cMAF and MAFB. Cases lacking an IgH translocation are associated with hyperdiploid phenotype. Know more at: http://www.creative-bioarray.com/IGH-CCND3-Translocation,-Dual-Fusion-Probe-FHPC-062-item-4703.htm