A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2743904



Internal ID9978188
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:1166323..1167327hg38UCSC Ensembl
Outerchr11:1159972..1160662hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg381005
hg19691
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6904731, essv6771880, essv6866884, essv6931630, essv6944695, essv6706036, essv6787572, essv6887854, essv6912401, essv6783368, essv6815294, essv6771879, essv6834707, essv6800006, essv6779263, essv6795833, essv6823435, essv6927760, essv6873524, essv6970587, essv6672844, essv6940122, essv6894481, essv6900484, essv6731925, essv6958955, essv6935920, essv6842259, essv6688123, essv6884948, essv6681403, essv6815295, essv6728145, essv6706035, essv6681406, essv6712822, essv6779264, essv6768351, essv6775541, essv6965465, essv6831118, essv6976795, essv6791660, essv6731922, essv6882171, essv6838440, essv6716602, essv6948870, essv6827497, essv6940121, essv6812073, essv6953023, essv6728146, essv6702238
SamplesSSM100, SSM083, SSM071, SSM027, SSM024, SSM046, SSM064, SSM079, SSM065, SSM039, SSM013, SSM042, SSM023, SSM028, SSM084, SSM021, SSM047, SSM069, SSM029, SSM096, SSM026, SSM089, SSM019, SSM035, SSM094, SSM031, SSM067, SSM033, SSM066, SSM068, SSM081, SSM040, SSM072, SSM082, SSM020, SSM015, SSM080, SSM077, SSM076, SSM022, SSM091, SSM070, SSM095, SSM025, SSM043, SSM098
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)esv2743904
Frequency
Sample Size96
Observed Gain0
Observed Loss46
Observed Complex0
Frequencyn/a


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