A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1036066



Internal ID19125285
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:5773003..5788219hg38UCSC Ensembl
Innerchr11:5794233..5809449hg19UCSC Ensembl
Innerchr11:5750809..5766025hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3815217
hg1915217
hg1815217
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1052n100
Supporting Variantsnssv3708489, nssv3509982, nssv3708490, nssv3511379, nssv3708482, nssv3708486, nssv3508661, nssv3517005, nssv3708479, nssv3708483, nssv3517902, nssv3513866, nssv3510190, nssv3708488, nssv3509219, nssv3708478, nssv3515242, nssv3513839, nssv3508030, nssv3504560, nssv3708480, nssv3510015, nssv3505840, nssv3504691, nssv3519341, nssv3519173, nssv3521858, nssv3515926, nssv3708485, nssv3708484, nssv3509421, nssv3504575, nssv3516962, nssv3520908, nssv3708477, nssv3708481, nssv3708491, nssv3505229, nssv3519007, nssv3513856, nssv3708487
Samples
Known GenesOR52N1, OR52N5
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1036066
Frequency
Sample Size11257
Observed Gain0
Observed Loss41
Observed Complex0
Frequencyn/a


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