Variant Details

Variant: esv2676255

Internal ID

9595674

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
Inner	chr1:23930426..23993032	hg38	UCSC Ensembl
Outer	chr1:23930055..23993402	hg38	UCSC Ensembl
Inner	chr1:24256916..24319522	hg19	UCSC Ensembl
Outer	chr1:24256545..24319892	hg19	UCSC Ensembl

Cytoband

1p36.11

Allele length

Assembly	Allele length
hg38	63348
hg19	63348

Variant Type

CNV deletion

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

Merged Variants

Supporting Variants

essv6263821, essv5460111, essv6470712, essv5543571, essv5568989, essv5502878, essv5815793, essv6223000, essv5535735, essv5696689, essv5834335, essv5657971, essv5775587, essv5458279, essv5685776, essv6133992, essv6150791, essv5641327, essv6065453, essv5826734, essv6502255, essv5846032, essv5839876, essv5632388, essv5854710, essv6419179, essv6530819, essv6205556, essv6223248, essv5420473, essv6471479, essv6267797, essv5652043, essv6029480, essv5776834, essv6032725, essv5523576, essv6174404, essv6285848, essv6407576, essv5468498, essv5935079, essv5556143, essv5553999, essv6329332, essv5491374, essv6008683, essv5741543, essv5589908, essv6541778, essv6038427, essv5640877, essv5837996

Samples

HG01060, HG01173, HG01098, HG01052, HG01079, HG01188, HG01066, HG00640, HG00737, HG01051, HG00641, HG01070, HG01167, HG01168, HG00736, HG01083, HG01069, HG01080, HG01067, HG01170, HG01072, HG01176, HG01198, HG00637, HG01048, HG01183, HG00731, HG01187, HG01171, HG00732, HG01095, HG00740, HG01047, HG01102, HG01073, HG01197, HG01182, HG01101, HG01107, HG01204, HG01075, HG01190, HG00734, HG00638, HG01174, HG01108, HG01055, HG01082, HG01097, HG00554, HG01191, HG01061, HG00553

Known Genes

PNRC2, SRSF10

Method

Merging

Analysis

No reference, merging analysis

Platform

Merging

Comments

Reference

1000_Genomes_Consortium_Phase_1

Pubmed ID

23128226

Accession Number(s)

esv2676255

Frequency

Sample Size	1151
Observed Gain	0
Observed Loss	53
Observed Complex	0
Frequency	n/a