A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2744349



Internal ID9978633
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:36756179..36756626hg38UCSC Ensembl
Outerchr11:36777729..36778176hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg38448
hg19448
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6827553, essv6737187, essv6870601, essv6731976, essv6720544, essv6686209, essv6894516, essv6833665, essv6931669, essv6891130, essv6706074, essv6740933, essv6915983, essv6716641, essv6724350, essv6795880, essv6688161, essv6912440, essv6728189, essv6976889, essv6806248, essv6864453, essv6944746, essv6969951, essv6897537, essv6834746, essv6803374, essv6879368
SamplesSSM071, SSM045, SSM046, SSM011, SSM097, SSM073, SSM093, SSM074, SSM023, SSM090, SSM047, SSM029, SSM035, SSM044, SSM040, SSM082, SSM020, SSM007, SSM015, SSM016, SSM005, SSM080, SSM010, SSM004, SSM099, SSM043, SSM052, 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)esv2744349
Frequency
Sample Size96
Observed Gain0
Observed Loss28
Observed Complex0
Frequencyn/a


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