A curated catalogue of human genomic structural variation




Variant Details

Variant: esv275584



Internal ID1804
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:128484465..128484477hg38UCSC Ensembl
Outerchr11:128484368..128484489hg38UCSC Ensembl
Innerchr11:128354360..128354372hg19UCSC Ensembl
Outerchr11:128354263..128354384hg19UCSC Ensembl
Innerchr11:127859570..127859582hg18UCSC Ensembl
Outerchr11:127859473..127859594hg18UCSC Ensembl
Cytoband11q24.3
Allele length
AssemblyAllele length
hg38122
hg19122
hg18122
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv2585237
Samples
Known GenesETS1
MethodSNP array
AnalysisIdentification of germline Changes in Copy Number (IgC2N)
PlatformAffymetrix SNP 6.0
Comments
ReferenceBanerjee_et_al_2011
Pubmed ID21479260
Accession Number(s)esv275584
Frequency
Sample Size1250
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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