Variant Details

Variant: esv2677334

Internal ID

9943439

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
Inner	chr4:23719143..23720199	hg38	UCSC Ensembl
Outer	chr4:23718772..23720569	hg38	UCSC Ensembl
Inner	chr4:23720766..23721822	hg19	UCSC Ensembl
Outer	chr4:23720395..23722192	hg19	UCSC Ensembl

Cytoband

4p15.2

Allele length

Assembly	Allele length
hg38	1798
hg19	1798

Variant Type

CNV deletion

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

Merged Variants

Supporting Variants

essv6444569, essv5472239, essv5862628, essv6259004, essv6572667, essv5790515, essv6467438, essv6473184, essv5470961, essv5959746, essv6371509, essv6451714, essv6524165, essv6186697, essv6451291, essv5650772, essv5555450, essv6414294, essv6229847, essv6244492, essv6197606, essv5799129, essv5419987, essv6403716, essv5879140, essv5807932, essv6249521, essv6470249, essv6366871, essv5890010, essv5743867, essv6284126, essv6361439, essv6254692, essv5561608, essv6082119, essv5407043, essv5720435, essv6494916, essv6006754, essv6073035, essv6413389, essv5451089, essv5842941, essv5581137, essv6555939, essv5399827, essv6404364, essv6542458, essv5487104, essv5757695, essv5402740, essv5868403

Samples

HG00189, HG00318, HG00177, HG00271, HG00272, HG00330, HG00346, HG00369, HG00270, HG00334, HG00185, HG00311, HG00281, HG00277, HG00309, HG00182, HG00338, HG00178, HG00323, HG00313, HG00268, HG00266, HG00328, HG00190, HG00320, HG00344, HG00324, HG00284, HG00273, HG00373, HG00331, HG00321, HG00276, HG00336, HG00285, HG00353, HG00357, HG00278, HG00319, HG00339, HG00269, HG00312, HG00329, HG00342, HG00267, HG00310, HG00186, HG00280, HG00343, HG00377, HG00372, HG00274, HG00345

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)

esv2677334

Frequency

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