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Mutational screening of CNL, aCML, and CMML. Alignment of gene mutations, cytogenetics, and entity information. Each column represents one of the 218 patients analyzed for CSF3R, SETBP1, SRSF2, TET2, ASXL1, CBL, and karyotype (shown in rows). Upper rows: red: mutated gene, light gray: non-mutated gene. Cytogenetics: dark gray: aberrant karyotype (n=54), light gray: normal karyotype (n=157). White: no data available.
