Small Deletion Variants Have Stable Breakpoints Commonly Associated with Alu Elements

Copy number variants (CNVs) contribute significantly to human genomic variation, with over 5000 loci reported, covering more than 18% of the euchromatic human genome. Little is known, however, about the origin and stability of variants of different size and complexity. We investigated the breakpoint...

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Autors principals: de Smith, Adam J., Walters, Robin G., Coin, Lachlan J. M., Steinfeld, Israel, Yakhini, Zohar, Sladek, Rob, Froguel, Philippe, Blakemore, Alexandra I. F.
Format: Article
Idioma:English
Publicat: Public Library of Science 2008
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Research Article
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC2518860/
https://ncbi.nlm.nih.gov/pubmed/18769679
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0003104
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https://ncbi.nlm.nih.gov/pmc/articles/PMC2518860/
https://ncbi.nlm.nih.gov/pubmed/18769679
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0003104

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