A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2744577



Internal ID10325547
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:60823744..60824299hg38UCSC Ensembl
Outerchr11:60591217..60591772hg19UCSC Ensembl
Cytoband11q12.2
Allele length
AssemblyAllele length
hg38556
hg19556
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6746747, essv6783452, essv6850990, essv6791742, essv6740960, essv6779337, essv6771946, essv6842317, essv6948958, essv6823527, essv6800086, essv6724387, essv6898231, essv6732012, essv6684978, essv6931709, essv6959080, essv6677696, essv6815358, essv6924213, essv6927826, essv6749587, essv6770843
SamplesSSM008, SSM024, SSM045, SSM079, SSM065, SSM084, SSM047, SSM018, SSM026, SSM019, SSM032, SSM067, SSM086, SSM068, SSM072, SSM020, SSM077, SSM055, SSM070, SSM034, SSM052, SSM056, SSM012
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)esv2744577
Frequency
Sample Size96
Observed Gain0
Observed Loss23
Observed Complex0
Frequencyn/a


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