A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2743889



Internal ID10324859
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:1076353..1076643hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg19291
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6866882, essv6672841, essv6850867, essv6771876, essv6904727, essv6746678, essv6831115, essv6706033, essv6965460, essv6749530, essv6720501, essv6775537, essv6842260, essv6823431, essv6927759, essv6907274, essv6833421
SamplesSSM027, SSM079, SSM065, SSM013, SSM002, SSM084, SSM089, SSM019, SSM031, SSM044, SSM086, SSM066, SSM081, SSM040, SSM010, SSM055, SSM056
Known GenesMUC2
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)esv2743889
Frequency
Sample Size96
Observed Gain0
Observed Loss17
Observed Complex0
Frequencyn/a


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