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...

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...

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

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...

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

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

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...

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

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...

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

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

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

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

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

genetic variants, (2015). Methods to detect rare mutations and copy number variation, (2016). Methods for multi-resolution analysis of cell-free nucleic...

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

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...

adapted to allow the precise analysis of copy-number variation, and in particular the analysis of copy-number changes in cancer. Dear PH, Cook PR (September...

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

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

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...

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

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

of genetic material from chromosome 7. The most common recurrent copy number variation disorder is DiGeorge syndrome (22q11.2 deletion syndrome), followed...

10–15% of autism cases may result from single gene disorders or copy number variations (CNVs)—spontaneous alterations in the genetic material during meiosis...

polymorphisms (SNPs), which are a big part of genetic variation in the human genome, and copy number variation (CNV), pose problems in single cell sequencing...

(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...

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

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