AUTHOR=Salehian-Dehkordi Hosein , Xu Ya-Xi , Xu Song-Song , Li Xin , Luo Ling-Yun , Liu Ya-Jing , Wang Dong-Feng , Cao Yin-Hong , Shen Min , Gao Lei , Chen Ze-Hui , Glessner Joseph T. , Lenstra Johannes A. , Esmailizadeh Ali , Li Meng-Hua , Lv Feng-Hua TITLE=Genome-Wide Detection of Copy Number Variations and Their Association With Distinct Phenotypes in the World’s Sheep JOURNAL=Frontiers in Genetics VOLUME=12 YEAR=2021 URL=https://www.frontiersin.org/journals/genetics/articles/10.3389/fgene.2021.670582 DOI=10.3389/fgene.2021.670582 ISSN=1664-8021 ABSTRACT=
Copy number variations (CNVs) are a major source of structural variation in mammalian genomes. Here, we characterized the genome-wide CNV in 2059 sheep from 67 populations all over the world using the Ovine Infinium HD (600K) SNP BeadChip. We tested their associations with distinct phenotypic traits by conducting multiple independent genome-wide tests. In total, we detected 7547 unique CNVs and 18,152 CNV events in 1217 non-redundant CNV regions (CNVRs), covering 245 Mb (∼10%) of the whole sheep genome. We identified seven CNVRs with frequencies correlating to geographical origins and 107 CNVRs overlapping 53 known quantitative trait loci (QTLs). Gene ontology and pathway enrichment analyses of CNV-overlapping genes revealed their common involvement in energy metabolism, endocrine regulation, nervous system development, cell proliferation, immune, and reproduction. For the phenotypic traits, we detected significantly associated (adjusted