A curated catalogue of human genomic structural variation

Variant Details

Variant: esv3892025

Internal ID

18839735

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
Inner	chr11:71675753..71814755	hg38	UCSC Ensembl
Outer	chr11:71570814..71849534	hg38	UCSC Ensembl
Inner	chr11:71386799..71525801	hg19	UCSC Ensembl
Outer	chr11:71281860..71560580	hg19	UCSC Ensembl
Inner	chr11:71064447..71203449	hg18	UCSC Ensembl
Outer	chr11:70959508..71238228	hg18	UCSC Ensembl

Cytoband

11q13.4

Allele length

Assembly	Allele length
hg38	278721
hg19	278721
hg18	278721

Variant Type

CNV gain

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

M

Merged Variants

Supporting Variants

essv25791859, essv25791993, essv25792156, essv25790929, essv25791351, essv25792433

Samples

Known Genes

ALG1L9P, DEFB108B, FAM86C1, KRTAP5-11, ZNF705E

Method

SNP array

Analysis

Platform

Illumina HumanHap 610

Comments

Reference

Suktitipat_et_al_2014

Pubmed ID

Accession Number(s)

Frequency

Sample Size	3017
Observed Gain	6
Observed Loss	0
Observed Complex	0
Frequency	n/a