A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv452083



Internal ID18274578
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55549600..55744786hg38UCSC Ensembl
Innerchr11:55317076..55512262hg19UCSC Ensembl
Innerchr11:55073652..55268838hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg38195187
hg19195187
hg18195187
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv428256
Supporting Variants
SamplesNA18916
Known GenesOR4C11, OR4C15, OR4C16, OR4C6, OR4P4, OR4S2
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)nssv452083
Frequency
Sample Size62
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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