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Copy Number Variants — Copy Number Variation. The gene copy number (also “copy number variants” or CNS) is the number of copies of a particular gene in the genotype of an individual. Recent evidence shows that the gene copy number can be elevated in cancer cells.
copy number. The number of copies of a particular PLASMID per CHROMOSOME present in a CELL. The number of copies of a GENE in the GENOME of an ORGANISM.
CNS are then detected based on the frequency of the reads (read depth) or aberrations in the mate pairs, after mapping the short reads to the reference genome. The majority of the current CNV detection tools analyze only one sample genome, at a time.
Plasmid copy number was determined by comparing the quantification signal from the plasmid to those from the chromosome. Copy number was then calculated by using a known copy number plasmid as a standard.
Refers to the genetic trait involving the number of copies of a particular gene present in the genome of an individual. Copy number variants account for a significant proportion of the genetic variation between individuals. Also called CNV.
The gene copy number (also “copy number variants” or CNS) is the number of copies of a particular gene in the genotype of an individual. Recent evidence shows that the gene copy number can be elevated in cancer cells. It was generally thought that genes were almost always present in two copies in a genome.
A copy number variation (CNV) is when the number of copies of a particular gene varies from one individual to the next. Following the completion of the Human Genome Project, it became apparent that the genome experiences gains and losses of genetic material.
Refers to the genetic trait involving the number of copies of a particular gene present in the genome of an individual. Genetic variants, including insertions, deletions, and duplications of segments of DNA, are also collectively referred to as copy number variants.
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