A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2745127



Internal ID10326097
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:118875456..118876186hg38UCSC Ensembl
Outerchr11:118746165..118746895hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg38731
hg19731
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6775638, essv6842368, essv6857103, essv6806325, essv6944864, essv6924265, essv6720623, essv6851068, essv6904855, essv6791788, essv6795967, essv6800142, essv6879434, essv6970735, essv6728266, essv6898655, essv6891222, essv6959158, essv6834826, essv6783508, essv6685023, essv6712925, essv6823568, essv6691535, essv6809317, essv6732062, essv6949022, essv6887960, essv6815412
SamplesSSM036, SSM071, SSM024, SSM075, SSM046, SSM079, SSM087, SSM097, SSM013, SSM093, SSM074, SSM042, SSM023, SSM028, SSM084, SSM047, SSM018, SSM096, SSM026, SSM044, SSM086, SSM066, SSM068, SSM072, SSM082, SSM077, SSM070, SSM034, 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)esv2745127
Frequency
Sample Size96
Observed Gain0
Observed Loss29
Observed Complex0
Frequencyn/a


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