A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2164n54



Internal ID22770059
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:107368380..107370809hg38UCSC Ensembl
chr11:107239106..107241535hg19UCSC Ensembl
chr11:106744316..106746745hg18UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg382430
hg192430
hg182430
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv556295, nsv556296, nsv556312, nsv556293, nsv556292, nsv556311, nsv556294
Samples
Known GenesCWF19L2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv2164n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss21
Observed Complex0
Frequencyn/a


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