Variant Details

Variant: esv3625679

Internal ID

7012513

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
	chr11:24636826..24642816	hg38	UCSC Ensembl
Inner	chr11:24636830..24642812	hg38	UCSC Ensembl
Outer	chr11:24636822..24642820	hg38	UCSC Ensembl
	chr11:24658372..24664362	hg19	UCSC Ensembl
Inner	chr11:24658376..24664358	hg19	UCSC Ensembl
Outer	chr11:24658368..24664366	hg19	UCSC Ensembl

Cytoband

11p14.3

Allele length

Assembly	Allele length
hg38	5991
hg19	5991

Variant Type

CNV loss

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

Merged Variants

Supporting Variants

essv14060149, essv14060180, essv14060163, essv14060146, essv14060172, essv14060161, essv14060173, essv14060155, essv14060150, essv14060184, essv14060160, essv14060170, essv14060144, essv14060166, essv14060156, essv14060141, essv14060159, essv14060147, essv14060186, essv14060168, essv14060157, essv14060140, essv14060182, essv14060178, essv14060181, essv14060176, essv14060179, essv14060174, essv14060175, essv14060171, essv14060148, essv14060143, essv14060164, essv14060185, essv14060162, essv14060154, essv14060183, essv14060151, essv14060165, essv14060158, essv14060169, essv14060142, essv14060177, essv14060152, essv14060153, essv14060145, essv14060167

Samples

NA20339, HG02583, HG03548, HG03300, HG01389, NA18917, HG02012, HG03518, HG03515, HG03139, HG02536, HG03133, HG03086, HG02485, NA18923, NA19198, HG03246, HG02054, HG03195, HG02946, HG03055, NA18908, HG02439, HG02582, HG02508, NA19114, NA18853, HG02635, NA19395, HG02568, HG01990, HG02455, NA18517, HG02837, NA19144, HG02982, HG03433, NA19467, HG03557, NA19143, HG03157, HG02970, NA19474, NA19213, HG01883, HG03445, NA18505

Known Genes

LUZP2

Method

Sequencing

Analysis

Platform

Multiple platforms

Comments

Reference

1000_Genomes_Consortium_Phase_3

Pubmed ID

21293372

Accession Number(s)

esv3625679

Frequency

Sample Size	2504
Observed Gain	0
Observed Loss	47
Observed Complex	0
Frequency	n/a