Examples of 'cnvs' in a sentence
Meaning of "cnvs"
CNVS is a term commonly abbreviated for 'Copy Number Variation Sequencing', a genomic technique used to detect variations in the number of copies of a particular region of DNA
Show more definitions
- plural of CNV
How to use "cnvs" in a sentence
Basic
Advanced
cnvs
Improves the detection of CNVs in regions of prognostic interest.
Larger DIPs may be treated as CNVs.
These same CNVs are also implicated in autism and schizophrenia.
It is also noteworthy that many of CNVs are not in coding regions.
Analysis of CNVs is fast becoming an integral part of an autism diagnosis.
Schizophrenia has also been associated with multiple de novo CNVs.
De novo CNVs in clinically significant gene regions are more likely to be causative.
These models will help interpreting CNVs identified in the clinic.
An accompanying paper looks at what the genes present in these CNVs do.
Cnvs can contribute to risk variability among individuals in complex diseases etiology.
Many of the regions in which the CNVs were identified overlapped known disease genes.
Previous studies have suggested that girls with autism tend to have larger CNVs than boys.
Along with SNPs these CNVs account for a significant amount of phenotypic variation between individuals.
The MLPA is an established technique for detecting known CNVs.
No pathogenic CNVs were reported in the isolated fetal IUGR group.
See also
ACGH from a sample of CLL with multiple CNVs.
Other CNVs or genetic mutations may also contribute to ADHD.
Table 3 reports all the CNVs identified in patients.
CNVs are common and usually appear as deletions or duplications of significant stretches of DNA.
Recent studies have shown that CNVs occur in significant proportion in patients with CHD.
CNVs that span multiple genes may affect other major organs beyond the heart.
These became known as copy number variants, or CNVs.
CNVs can be nonrecurrent and recurrent.
The particular position of those CNVs on the chromosome?
CNVs are deletions or duplications of DNA sequences.
None of them presented changes similar to their children 's CNVs.
Some CNVs have an impact on the neuro-development.
This low frequency implies that, with a larger population, even rarer CNVs would be uncovered.
Rare CNVs may also contribute to early-onset obesity.
These metastases, however, did not have a significantly larger number of CNVs than the primary tumors.
Additionally, CNVs are perfused by a slower flow than the normal choriocapillaris.
Several studies have demonstrated the presence of CNVs in non-syndromic CHD.
These 55 CNVs were classified into three groups based on their clinical interpretation.
Table 2 provides a list of common CNVs which are characteristic of in recipient DNA.
CNVs can be caused by genomic rearrangements such as deletions, duplications, and translocations.
Currently, several studies have established the relevance of CNVs in the etiology of CHD.
However, many of the CNVs disrupted genes have never been linked to autism before.
The researchers identified 30 genes within these CNVs.
In LR DLBCLs, CNVs are related to immune response and cell proliferation.
Copy number variant analysis of 18 cell samples for several thousand CNVs.
CNVs will often contain genes, so they create differences in the dose of these genes.
In an embodiment, the CNVs are CNDs as listed in Table 3.
CNVs are mentioned with the chromosomal band ( s ) they involve and their genome sequence coordinates.
In addition, CONTRA provides gene-specific information on CNVs.
CNVs are detected by fluorescence in situ hybridization ( FISH ) or comparative genomic hybridization CGH.
Based on the published literature, MECP2 is the most autism-associated gene among the identified CNVs.
CNVs have been associated with various forms of cancer Cappuzzo F, Hirsch, et al.
Cases and controls each had 2.4 CNVs on average.
Thirteen CNVs were identified in 12 individuals.
The ages of the seven patients who presented CNVs ranged from 19 days to 10 years.
