A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv428267



Internal ID18278031
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:132131883..132223561hg38UCSC Ensembl
Innerchr11:132001777..132093455hg19UCSC Ensembl
Innerchr11:131506987..131598665hg18UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg3891679
hg1991679
hg1891679
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv452218, nssv452217, nssv452216, nssv452215
SamplesHGDP00462, NA19181, NA19189, NA19113
Known GenesNTM
MethodBAC aCGH
AnalysisCopy number variable segments were automatically detected using the CNVfinder algorithm (Fiegler et al. 2006).
PlatformSanger H. sapiens Whole Genome Tile Path 28.7k v3
Comments
ReferencePerry_et_al_2008b
Pubmed ID18775914
Accession Number(s)nsv428267
Frequency
Sample Size62
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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