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Fig. 2 | Genome Medicine

Fig. 2

From: Whole genome sequencing reveals the independent clonal origin of multifocal ileal neuroendocrine tumors

Fig. 2

A minimally targeted region on chr18q12.2. A Integrative Genomics Viewer (IGV) view of a 148 kb deletion at chr18q12.2 in a primary ileal NET. The deletion overlaps with a part of a gene, KIAA1328, and a part of an intergenic region between KIAA1328 and the adjacent gene, CELF4. B The copy ratio and allele fraction segments. C IGV view of the sequencing reads at the breakpoints of the deletion. The reads are colored by insert size. Reads that are colored red have larger than expected inferred sizes, indicating a deletion

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