{"id":"W2034197594","doi":"10.1038/nrg3871","title":"A copy number variation map of the human genome","year":2015,"lang":"en","type":"review","venue":"Nature Reviews Genetics","topic":"Genomic variations and chromosomal abnormalities","field":"Biochemistry, Genetics and Molecular Biology","cited_by":987,"is_retracted":false,"has_abstract":false,"ca_institutions":"University of Toronto; Hospital for Sick Children","funders":"","keywords":"Biology; Copy-number variation; Genome; Genetics; Phenotype; Human genome; Gene; Human genetic variation; Ploidy; Evolutionary biology; Computational biology","routes":{"ca_aff":true,"ca_fund":false,"ca_venue":false,"about_ca":false,"invisible_to_affiliation_only":false},"retraction":null,"screen":null,"machine_scores":{"provisional":true,"baseline":true,"maturity_gate_passed":false,"score_opus":0.02970703466678725,"score_gpt":0.3356524094560503,"score_spread":0.3059453747892631,"validation_status":"score_only:v0-immature-baseline","note":"Baseline scores from an immature model (maturity gate not passed). Scores rank; they never assert a category."}}