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...

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...

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

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...

RCCX is a complex, multiallelic, and tandem copy number variation (CNV) human DNA locus on chromosome 6p21.3, a cluster located in the major histocompatibility...

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...

in a case where it is a rare genetic variant Copy-number variation Variant (biology) Genetic variation (disambiguation) Polymorphism (biology), the effect...

human gene copy number variation. Nat Genet. 2007; 39: 1256–60 *Co-senior authors 2007: Lee C, Iafrate AJ, Brothman AR. Copy number variations and clinical...

substitution and indels. Large-scale structural variation (>1 kb) can be either copy number variation (loss or gain), or chromosomal rearrangement (translocation...

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

specific chromosomes or chromosomal abnormalities. DNA copy number variation: DNA copy number variation can be measured using flow cytometry techniques such...

aberration. Before analyzing target genome structural aberration and copy number variation (CNV) with ESP, the target genome is usually amplified and conserved...

regions in the human genome, is highly susceptible to copy number variation due to its frequent low-copy duplications. Whole exon sequencing and quantitative...

Nationaal Vakverbond in Dutch Trade Unions Copy number variation in genetics contingent negative variation in evoked potentials Cranial nerve V, also...

and disease phenotype is present. Copy number variation (CNV) refers to the differences in the number of copies of a particular region of the genome...

loss or increased copy number of genes within the deleted or duplicated region. It can also contribute to the copy number variation seen in some gene...

C4B genes usually in tandem RCCX cassettes with copy number variation, that somewhat parallels variation in the levels of their respective proteins within...

hybridization (CGH) is a molecular cytogenetic method for analysing copy number variations (CNVs) relative to ploidy level in the DNA of a test sample compared...

interrupt the genome through insertions, deletions, rearrangements, and copy number variations. L1 activity has contributed to the instability and evolution of...

(2015-10-08). "Single molecule sequencing of THCA synthase reveals copy number variation in modern drug-type Cannabis sativa L": 028654. doi:10.1101/028654...

and host genomes using deep sequencing datasets. CNVseq detects copy number variations supported on a statistical model derived from array-comparative...

AC (October 2007). "Diet and the evolution of human amylase gene copy number variation". Nature Genetics. 39 (10): 1256–1260. doi:10.1038/ng2123. PMC 2377015...

the deletion is situated. The syndrome is a form of the 1q21.1 copy number variations, and it is a deletion in the distal area of the 1q21.1 part. The...

aids in detecting copy number variations, single nucleotide polymorphisms (SNPs), indels, and other genomic structural variations. Virtually started...

Representational oligonucleotide microarray analysis: Detects copy number variation using amplified restriction-digested genomic fragments that are...

genomic copy number variation in cancer and other genetic diseases. In this technique, two genomes are compared for their differences in copy number on a...