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. Author manuscript; available in PMC: 2013 Nov 13.
Published in final edited form as: Cancer Cell. 2012 Nov 13;22(5):683–697. doi: 10.1016/j.ccr.2012.10.007

Figure 2. Somatic mutations in whole genome sequenced AMKL cases.

Figure 2

Plots depict structural genetic variants, including DNA copy number alterations, intraand inter-chromosomal translocations, and sequence alterations (Krzywinski et al., 2009). DNA copy number alterations: Loss of heterozygosity (LOH), orange; amplification, red; deletion, blue. Sequence mutations in Refseq genes: silent single nucleotide variants (SNVs), black; UTR, brown; non-silent SNVs, blue. Genes at structural variant breakpoints: genes involved in in-frame fusions, red; others, green.