A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6834499



Internal ID10006242
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:134045831..134046560hg38UCSC Ensembl
Outerchr11:133915726..133916455hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg38730
hg19730
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2745311
Supporting Variants
SamplesSSM010
Known Genes
MethodSequencing
AnalysisBreakdancer:4 times standard deviation,VariationHunter:4 times standard deviation and at least 3 supportting reads
PlatformIllumina HiSeq 2000
Comments
ReferenceWong_et_al_2012b
Pubmed ID23290073
Accession Number(s)essv6834499
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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