Copy number variation (CNV) contributes significantly to natural genetic variation within and between populations. However, the mutational mechanisms leading to CNV, as well as the processes that control the size of CNV regions, are so far not well understood. Here, we have analyzed a gene family that forms CNV regions on the X and the Y chromosomes in Mus musculus. These CNV regions show copy number differences in two subspecies, M. musculus domesticus and M. musculus musculus. Assessment of copy numbers at these loci for individuals caught in a natural hybrid zone showed copy number increases and a large variance among individuals. Crosses of natural hybrid animals among each other produced even more extreme variants with major difference...
BACKGROUND: Copy number variation is an important dimension of genetic diversity and has implication...
Background: Copy number variation is an important dimension of genetic diversity and has implication...
Copy number variants (CNVs) are a source of genomic variation associated with altered phenotypes. So...
Copy number variation (CNV) contributes significantly to natural genetic variation within and betwee...
Copy number variation (CNV) contributes significantly to natural genetic variation within and betwee...
Different species, populations and individuals vary considerably in the copy number of discrete segm...
Copy number variation represents a major source of genetic divergence, yet the evolutionary dynamics...
Array comparative genomic hybridization (aCGH) to detect copy number variants (CNVs) in mammalian ge...
Array comparative genomic hybridization (aCGH) to detect copy number variants (CNVs) in mammalian ge...
Copy number variants (CNVs) are genomic segments which are duplicated or deleted among different ind...
Copy–numbervariants(CNVs)mayplayanimportantroleinearlyadaptations,potentiallyfacilitatingrapiddiverg...
Copy number variants (CNVs) are thought to underlie many human developmental abnormalities. However,...
Submicroscopic (less than 2 Mb) segmental DNA copy number changes are a recently recognized source o...
Abstract Hybrid zones between divergent populations sieve genomes into blocks that introgress across...
Copy number variants (CNVs) are thought to underlie many human developmental abnormalities. However,...
BACKGROUND: Copy number variation is an important dimension of genetic diversity and has implication...
Background: Copy number variation is an important dimension of genetic diversity and has implication...
Copy number variants (CNVs) are a source of genomic variation associated with altered phenotypes. So...
Copy number variation (CNV) contributes significantly to natural genetic variation within and betwee...
Copy number variation (CNV) contributes significantly to natural genetic variation within and betwee...
Different species, populations and individuals vary considerably in the copy number of discrete segm...
Copy number variation represents a major source of genetic divergence, yet the evolutionary dynamics...
Array comparative genomic hybridization (aCGH) to detect copy number variants (CNVs) in mammalian ge...
Array comparative genomic hybridization (aCGH) to detect copy number variants (CNVs) in mammalian ge...
Copy number variants (CNVs) are genomic segments which are duplicated or deleted among different ind...
Copy–numbervariants(CNVs)mayplayanimportantroleinearlyadaptations,potentiallyfacilitatingrapiddiverg...
Copy number variants (CNVs) are thought to underlie many human developmental abnormalities. However,...
Submicroscopic (less than 2 Mb) segmental DNA copy number changes are a recently recognized source o...
Abstract Hybrid zones between divergent populations sieve genomes into blocks that introgress across...
Copy number variants (CNVs) are thought to underlie many human developmental abnormalities. However,...
BACKGROUND: Copy number variation is an important dimension of genetic diversity and has implication...
Background: Copy number variation is an important dimension of genetic diversity and has implication...
Copy number variants (CNVs) are a source of genomic variation associated with altered phenotypes. So...