Variant Details

Variant: esv2659018

Internal ID

9925123

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
	chr5:149327060..149327300	hg38	UCSC Ensembl
	chr5:148706623..148706863	hg19	UCSC Ensembl

Cytoband

5q32

Allele length

Assembly	Allele length
hg38	241
hg19	241

Variant Type

CNV deletion

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

Merged Variants

Supporting Variants

essv5835553, essv5767304, essv5947024, essv6584784, essv6366372, essv5456474, essv5462909, essv6446831, essv6037000, essv6427729, essv5930277, essv5713186, essv5620415, essv6066995, essv5795218, essv6470098, essv6210714, essv5591400, essv6014330, essv6567113, essv6104849, essv6235486, essv5859184, essv6279461, essv6339419, essv5949821, essv6469135, essv6309135, essv5543127, essv6031847, essv6057102, essv5921435, essv5535891, essv5426518, essv6512128, essv5957023, essv6051719, essv6358491, essv6025005, essv5724029, essv5427564, essv6167220, essv5961947, essv5618754, essv5881236, essv5823957, essv5814190, essv6298696, essv6300487, essv6521620, essv6491768, essv5512402, essv6458509, essv6161570, essv5479179, essv5406193, essv6485173, essv6343259, essv6327089, essv6230321, essv5606319, essv6054061, essv5641750, essv5755914, essv5821352, essv6317584, essv6146280, essv6535820, essv6075853, essv5587480, essv5724546, essv5974743, essv5819407, essv5418629, essv5749841, essv6403326, essv5476912, essv6556372, essv6132216, essv5863393, essv5544348, essv5921878, essv6192729, essv6487189

Samples

HG00536, NA19397, NA18947, NA11995, NA20783, NA12843, HG00315, NA12045, NA18486, NA19355, NA19393, NA20332, HG00737, NA19067, HG00271, HG00663, NA18563, HG00641, NA19373, NA18550, NA18597, NA19762, NA12348, NA19088, NA18571, HG00185, NA19384, NA18949, HG01134, HG01455, NA19372, NA19385, NA18986, HG00427, NA12828, HG00323, HG00419, HG00543, NA18544, NA19210, NA12489, NA19657, HG01384, HG00657, HG00584, NA20126, NA18572, HG00708, NA12829, NA18499, NA11894, HG00684, NA18856, NA18912, NA19099, NA19452, NA19225, NA18593, NA19675, NA19375, HG00254, NA18909, NA18961, NA18559, NA18564, HG00353, HG00375, NA19435, NA19144, HG00473, NA20778, NA19470, NA19428, NA18610, NA18501, NA19093, NA19116, HG00595, HG00472, NA18488, NA18522, HG00437, HG00581, NA18620

Known Genes

AFAP1L1

Method

Merging

Analysis

No reference, merging analysis

Platform

Merging

Comments

Reference

1000_Genomes_Consortium_Phase_1

Pubmed ID

23128226

Accession Number(s)

esv2659018

Frequency

Sample Size	1151
Observed Gain	0
Observed Loss	84
Observed Complex	0
Frequency	n/a