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Identification of Copy Number Variation Hotspots in Human Populations
Copy number variants (CNVs) in the human genome contribute to both Mendelian and complex traits as well as to genomic plasticity in evolution. The investigation of mutational rates of CNVs is critical to understanding genomic instability and the etiology of the copy number variation (CNV)-related tr...
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| Main Authors: | , , , , |
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| Formáid: | Artigo |
| Teanga: | Inglês |
| Foilsithe: |
Elsevier
2010
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| Ábhair: | |
| Rochtain Ar Líne: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2948802/ https://ncbi.nlm.nih.gov/pubmed/20920665 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.ajhg.2010.09.006 |
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