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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...
Autores principales: | , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2008
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2518860/ https://www.ncbi.nlm.nih.gov/pubmed/18769679 http://dx.doi.org/10.1371/journal.pone.0003104 |