A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1967n54



Internal ID20135391
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:64709578..64817487hg38UCSC Ensembl
chr11:64477050..64584959hg19UCSC Ensembl
chr11:64233626..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 StatusM
Merged Variants
Supporting Variantsnsv555202, nsv555203
Samples1782681313_A, 1780862093_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)dgv1967n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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