Variant Details

Variant: esv2660771

Internal ID

9926876

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
	chr1:13836598..13840507	hg38	UCSC Ensembl
	chr1:14163093..14167002	hg19	UCSC Ensembl

Cytoband

1p36.21

Allele length

Assembly	Allele length
hg38	3910
hg19	3910

Variant Type

CNV deletion

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

Merged Variants

Supporting Variants

essv6344862, essv5446129, essv5913446, essv5470781, essv6100642, essv6563699, essv6276590, essv6289637, essv5688053, essv5561509, essv5614058, essv6334563, essv6569919, essv5508810, essv6007775, essv6112891, essv6030971, essv6586520, essv5738996, essv5878578, essv6326609, essv5947056, essv6475055, essv6414672, essv6499202, essv5638046, essv6113322, essv6057318, essv5712320, essv5660168, essv5456701, essv6556082, essv6241574, essv6546952, essv5663105, essv5421703, essv6591425, essv6198786, essv5601272, essv6208975, essv6101699, essv6479979, essv5881645, essv5638982, essv6143653, essv5850685, essv6150516, essv5653858, essv5617103, essv6131673, essv6064476, essv6302125, essv5837003, essv5652186

Samples

NA19394, NA19703, HG01188, NA19092, NA18486, NA19443, NA19107, NA19374, NA19381, NA19373, NA19171, NA19382, NA19916, NA20287, NA19130, NA19383, NA19137, NA19456, NA19437, NA19707, NA19403, NA19462, NA19347, NA19391, NA19982, NA20126, NA18871, NA18907, NA19449, HG01197, NA19453, NA19099, NA19257, NA19452, NA19225, NA19469, NA19318, NA18858, NA19440, NA19390, NA19147, NA18517, NA19712, NA19473, HG01551, NA19444, NA19470, NA18501, NA19093, NA18505, NA19316, NA18511, NA18487, NA19431

Known Genes

Method

Merging

Analysis

No reference, merging analysis

Platform

Merging

Comments

High quality site

Reference

1000_Genomes_Consortium_Phase_1

Pubmed ID

23128226

Accession Number(s)

esv2660771

Frequency

Sample Size	1151
Observed Gain	0
Observed Loss	54
Observed Complex	0
Frequency	n/a