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High resolution discovery and confirmation of copy number variants in 90 Yoruba Nigerians
BACKGROUND: Copy number variants (CNVs) account for a large proportion of genetic variation in the genome. The initial discoveries of long (> 100 kb) CNVs in normal healthy individuals were made on BAC arrays and low resolution oligonucleotide arrays. Subsequent studies that used higher resolutio...
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Main Authors: | , , , , |
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Formato: | Artigo |
Idioma: | Inglês |
Publicado em: |
BioMed Central
2009
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Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3091319/ https://ncbi.nlm.nih.gov/pubmed/19900272 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/gb-2009-10-11-r125 |
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