Copy number variations (CNVs) are important forms of structural variation in human and
animals and can be considered as a major genetic component of phenotypic diversity. Here …

Background Copy number variation (CNV) is a major source of structural variants and has
been commonly identified in mammalian genome. It is associated with gene expression and …

Copy number variations (CNVs) are important forms of genetic variation complementary to
SNPs, and can be considered as promising markers for some phenotypic and economically …

Copy number variations (CNVs) are one of the main contributors to genetic diversity in
animals and are broadly distributed in the genomes of swine. Investigating the performance …

Background Recent studies in pigs have detected copy number variants (CNVs) using the
Comparative Genomic Hybridization technique in arrays designed to cover specific porcine …

Copy number variation (CNV) is an important source of genetic variability in human or
animal genomes and play key roles in phenotypic diversity and disease susceptibility. In the …

Objective Copy number variations (CNVs) are a major source of genetic diversity
complementary to single nucleotide polymorphism (SNP) in animals. The aim of the study …

Objective Copy number variations (CNVs) are a major source of genetic diversity
complementary to single nucleotide polymorphism (SNP) in animals. The aim of the study …

Background Recent studies have shown that copy number variation (CNV) in mammalian
genomes contributes to phenotypic diversity, including health and disease status. In …

Abstract Background Copy Number Variations (CNVs) have been shown important in both
normal phenotypic variability and disease susceptibility, and are increasingly accepted as …