Chia, NicoleBryce, MichaelaHickman, PeterPotter, JuliaGlasgow, NicholasKoerbin, GusDanoy, PBrown, M. ACavanaugh, Juleen2015-12-131424-8581http://hdl.handle.net/1885/74037Copy number variations (CNVs) as described in the healthy population are purported to contribute significantly to genetic heterogeneity. Recent studies have described CNVs using lymphoblastoid cell lines or by application of specifically developed algoritKeywords: algorithm; Alu sequence; article; centromere; chromosome 18; chromosome analysis; chromosome size; consensus sequence; controlled study; copy number variation; DNA microarray; gene frequency; genetic association; genomic instability; high density single n Chromosome 18; Microhomology; Sequence; SNP microarray201310.1159/0003507672016-02-24