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A genome-wide assessment of rare copy number variants in colorectal cancer

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Figure

Figure 1: Outline of CNV discovery and CNV analysis. A total of 1004 sporadic CRC cases and 1994 controls were genotyped using Illumina Human-Omni Express BeadChip
Table 2: Global burden of rare CNVs between colorectal cases and controls
Table 3: Global burden of genic rare CNVs between colorectal cases and controls
Figure 2: Genome-wide burden of rare non-genic CNVs and genic CNVs. Genome-wide frequency of rare genic CNVs and rare non-genic CNVs were calculated for controls, rectal cancer patients and colon cancer patients respectively
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