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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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Detalles Bibliográficos
Autores principales:	Matsuzaki, Hajime, Wang, Pei-Hua, Hu, Jing, Rava, Rich, Fu, Glenn K
Formato:	Texto
Lenguaje:	English
Publicado:	BioMed Central 2009
Materias:	Research
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3091319/ https://www.ncbi.nlm.nih.gov/pubmed/19900272 http://dx.doi.org/10.1186/gb-2009-10-11-r125

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