A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1174809



Internal ID15507688
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:64709578..64817487hg38UCSC Ensembl
Innerchr11:64477050..64584959hg19UCSC Ensembl
Innerchr11:64233626..64341535hg18UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg38107910
hg19107910
hg18107910
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv555203
Supporting Variants
Samples1780862093_A
Known GenesMAP4K2, MEN1, NRXN2, PYGM, RASGRP2, SF1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1174809
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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