A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892014



Internal ID19186410
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55954749..56357467hg38UCSC Ensembl
Outerchr11:55954749..56357467hg38UCSC Ensembl
Innerchr11:55722225..56124943hg19UCSC Ensembl
Outerchr11:55722225..56124943hg19UCSC Ensembl
Innerchr11:55478801..55881519hg18UCSC Ensembl
Outerchr11:55478801..55881519hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg38402719
hg19402719
hg18402719
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25780261
Samples
Known GenesOR10AG1, OR5AS1, OR5F1, OR5J2, OR5T1, OR5T2, OR5T3, OR7E5P, OR8H1, OR8H2, OR8H3, OR8I2, OR8J3, OR8K1, OR8K3, OR8K5
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892014
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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