A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv556343



Internal ID16343752
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:107369523..107370809hg38UCSC Ensembl
Innerchr11:107240249..107241535hg19UCSC Ensembl
Innerchr11:106745459..106746745hg18UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg381287
hg191287
hg181287
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2170n54
Supporting Variantsnssv784164, nssv784163, nssv784165
Samples
Known GenesCWF19L2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv556343
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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