A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6904772



Internal ID9669693
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:45101672..45102060hg38UCSC Ensembl
Outerchr11:45123223..45123611hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg38389
hg19389
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2744421, esv2744422
Supporting Variants
SamplesSSM013
Known GenesPRDM11
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)essv6904772
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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