A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6800078



Internal ID10202306
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:56700565..56740248hg38UCSC Ensembl
Outerchr11:56468041..56507724hg19UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg3839684
hg1939684
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2744543
Supporting Variants
SamplesSSM072
Known GenesOR9G1, OR9G9
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)essv6800078
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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