{"id":"W2021714239","doi":"10.1038/nature08516","title":"Origins and functional impact of copy number variation in the human genome","year":2009,"lang":"en","type":"article","venue":"Nature","topic":"Genomic variations and chromosomal abnormalities","field":"Biochemistry, Genetics and Molecular Biology","cited_by":2051,"is_retracted":false,"has_abstract":false,"ca_institutions":"University of Toronto; Hospital for Sick Children","funders":"National Human Genome Research Institute; Canadian Institutes of Health Research; National Institute of General Medical Sciences; Nederlandse Organisatie voor Wetenschappelijk Onderzoek; Wellcome Trust","keywords":"Copy-number variation; Genetics; Biology; International HapMap Project; Human genome; Single-nucleotide polymorphism; Linkage disequilibrium; Genome; Genome-wide association study; 1000 Genomes Project; Structural variation; Locus (genetics); Genomics; Genotype; Gene","routes":{"ca_aff":true,"ca_fund":true,"ca_venue":false,"about_ca":false,"invisible_to_affiliation_only":false},"retraction":null,"screen":null}