High-resolution mapping and analysis of copy number variations in the human genome: A data resource for clinical and research applications

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Figure 3.
Figure 3.

Copy number variation within 15q13.3. Nonunique CNVs detected in our control data set that map within 15q13.3 (chr15:28,700,577–30,302,218, hg17, NCBI build 35) are shown as custom tracks within the UCSC Genome Browser (http://genome.ucsc.edu/). (Red rectangles) Deletions; (blue rectangles) duplications; (green rectangle) the CNV reported by Sharp et al. (2008). The UCSC known genes and segmental duplication tracks are also shown.

This Article

  1. Published in Advance July 10, 2009, doi: 10.1101/gr.083501.108 Genome Res. 19: 1682-1690

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