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Recurrent genomic aberrations in mantle cell lymphoma patients. Mantle cell lymphoma (MCL) has t(11;14)(q13;q32) resulting in a BCL1/CCND1 translocation with the immunoglobulin heavy chain (IgH) gene (IgH‐BCL1/CCND1).( 11 ) Array comparative genomic hybridization (CGH) analysis revealed that non‐random copy number aberrations also occurred in MCL patients.( 14 )
