Nat.%20Rev.%20Gen.%20CNV%20Map%20-%20Inclusive%20%28blue%3DGain%3B%20red%3DLoss%3B%20brown%3DGain%2BLoss%29

Copy number variation (CNV) accounts for much of the variability across genomes and can influence phenotypes. In this analysis, the authors construct a CNV map using high-quality data from published studies to provide more detailed insights into CNV, which will be useful for both clinical and research applications in the future. If using this data in your research, please cite the following: Zarrei M, MacDonald JR, Merico D, Scherer SW. A copy number variation map of the human genome. Nat Rev Genet. 2015 Feb 3. doi: 10.1038/nrg3871. [Epub ahead of print] PubMed PMID: 25645873.