Copy number variation (CNV) is a phenomenon in which sections of the genome are repeated and the number of repeats in the genome varies between individuals...

differences due to mutations occurring during development and gene copy-number variation. Differences between individuals, even closely related individuals...

have two doses -- one copy from the mother and one from the father. Changes in gene dosage can be a result of copy number variation (gene insertions or...

Genomic structural variation is the variation in structure of an organism's chromosome, such as deletions, duplications, copy-number variants, insertions...

variation in copy number in the human genome which questioned the characteristics of copy number variants in the human genome. It was known that copy...

1q21.1 copy number variations (CNVs) are rare aberrations of human chromosome 1. In a common situation a human cell has one pair of identical chromosomes...

Copy number analysis is the process of analyzing data produced by a test for DNA copy number variation in an organism's sample. One application of such...

method has been demonstrated as useful for studying variations in gene sequences — such as copy number variants and point mutations. The polymerase chain...

compared to an annotated database. Copy-number variations (CNVs) are an abundant form of genome structure variation in humans. A discrete-valued bivariate...

for instance, can be used to capture targets for SNPgenotyping, copy number variation or allelic imbalance studies, to name a few. In SNP genotyping,...