Figure 2.

Distribution of frequent mutations in CLL. Red boxes indicate which patients carry somatic mutations in any of the 50 most frequently mutated genes in CLL from two whole-exome studies: Quesada et al. (2011) (case ID in black) and Wang et al. (2011) (case ID in blue) ([24,25], respectively). Red boxes also indicate whether the patient was treated before sample collection (Chemotherapy), whether deletion of 13q14 was detected (13q14_del), and whether the disease was classified as IGHV-unmutated (IGHV-Unmut).

Quesada et al. BMC Medicine 2013 11:124   doi:10.1186/1741-7015-11-124
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