A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv777169



Internal ID16071125
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:64793728..64808033hg38UCSC Ensembl
Innerchr11:64561200..64575505hg19UCSC Ensembl
Innerchr11:64317776..64332081hg18UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg3814306
hg1914306
hg1814306
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv555205
Supporting Variants
Samples
Known GenesMAP4K2, MEN1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv777169
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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