A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv771088



Internal ID16065044
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:38227656..38286863hg38UCSC Ensembl
Innerchr11:38249206..38308413hg19UCSC Ensembl
Innerchr11:38205782..38264989hg18UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg3859208
hg1959208
hg1859208
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv554031
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv771088
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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