A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25788268



Internal ID18834240
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:48021501..49282806hg38UCSC Ensembl
Innerchr11:48043053..49304358hg19UCSC Ensembl
Innerchr11:47999629..49260934hg18UCSC Ensembl
Cytoband11p11.12
Allele length
AssemblyAllele length
hg381261306
hg191261306
hg181261306
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891986
Supporting Variants
Samples
Known GenesFOLH1, OR4A47, OR4B1, OR4C3, OR4C45, OR4S1, OR4X1, OR4X2, PTPRJ, TRIM49B, TRIM64C
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=103
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25788268
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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