A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2188n54



Internal ID20135612
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:125205679..125211544hg38UCSC Ensembl
chr11:125075575..125081440hg19UCSC Ensembl
chr11:124580785..124586650hg18UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg385866
hg195866
hg185866
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv556498, nsv556505, nsv556511, nsv556517, nsv556512, nsv556491, nsv556504
Samples
Known GenesPKNOX2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv2188n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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