Variant Details

Variant: esv2672644

Internal ID

9938749

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
Inner	chr15:70095777..70101983	hg38	UCSC Ensembl
Outer	chr15:70095406..70102453	hg38	UCSC Ensembl
Inner	chr15:70388116..70394322	hg19	UCSC Ensembl
Outer	chr15:70387745..70394792	hg19	UCSC Ensembl

Cytoband

15q23

Allele length

Assembly	Allele length
hg38	7048
hg19	7048

Variant Type

CNV deletion

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

Merged Variants

Supporting Variants

essv6050740, essv6063193, essv6442705, essv5501112, essv6537278, essv5838093, essv5580420, essv5542090, essv6203698, essv5620511, essv6140812, essv6079958, essv5752152, essv6130368, essv6551074, essv6302596, essv5418433, essv6430900, essv6363844, essv6370697, essv6455631, essv5837901, essv6481292, essv5834520, essv6058572, essv5985297, essv6383914, essv6081936, essv5778111, essv5709553, essv5745672, essv6172608, essv5824338, essv5872854, essv6172592, essv5746525, essv5564202, essv6218422, essv5727344, essv5688347, essv5451505, essv6157877, essv5410757, essv6080438, essv5910733, essv5509620, essv6248805, essv5426253, essv6249064, essv5534895, essv5398525, essv6270436, essv5465964, essv6039449, essv5688729, essv5935921, essv5888659, essv6037095, essv5835168, essv5503251, essv6276978, essv5670773, essv6044827, essv5399268, essv5934697, essv6014895, essv6251192, essv5866141, essv5828800, essv6301384, essv5925472, essv6217467, essv5844621, essv6554227, essv6101786, essv5488924, essv5918186, essv5801851, essv6286956, essv6271610

Samples

HG00187, NA18565, NA18599, HG00181, NA18530, NA18606, NA18616, NA18602, NA18627, HG00337, HG00327, HG00271, HG00272, NA18597, NA18595, NA18635, NA18567, HG00330, NA18574, HG00346, HG00270, HG00281, HG00277, HG00335, NA18560, NA18617, HG00309, HG00182, HG00338, HG00326, HG00178, HG00323, NA18539, NA18614, HG00313, NA18613, HG00176, HG00282, HG00328, HG00368, HG00320, HG00344, NA18637, HG00275, NA18534, NA18630, NA18548, HG00324, HG00284, HG00273, NA18626, HG00373, HG00331, NA18536, NA18541, NA18546, NA18632, HG00336, HG00285, NA18543, NA18559, HG00366, HG00353, NA18628, HG00278, HG00319, NA18615, NA18610, HG00312, NA18631, HG00329, HG00342, NA18636, HG00310, HG00186, HG00280, HG00343, HG00274, NA18612, NA18620

Known Genes

TLE3

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)

esv2672644

Frequency

Sample Size	1151
Observed Gain	0
Observed Loss	80
Observed Complex	0
Frequency	n/a