A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv777141



Internal ID15724411
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:63080046..63343097hg38UCSC Ensembl
Innerchr11:62847518..63110569hg19UCSC Ensembl
Innerchr11:62604094..62867145hg18UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg38263052
hg19263052
hg18263052
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv555177
Supporting Variants
Samples
Known GenesMIR3680-1, MIR3680-2, SLC22A10, SLC22A24, SLC22A25
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv777141
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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