Variant Details

Variant: esv3633551

Internal ID

7020360

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
	chr13:110934843..110936653	hg38	UCSC Ensembl
Inner	chr13:110934846..110936650	hg38	UCSC Ensembl
Outer	chr13:110934840..110936656	hg38	UCSC Ensembl
	chr13:111587190..111589000	hg19	UCSC Ensembl
Inner	chr13:111587193..111588997	hg19	UCSC Ensembl
Outer	chr13:111587187..111589003	hg19	UCSC Ensembl

Cytoband

13q34

Allele length

Assembly	Allele length
hg38	1811
hg19	1811

Variant Type

CNV loss

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

Merged Variants

Supporting Variants

essv14898084, essv14898082, essv14898038, essv14898064, essv14898100, essv14898094, essv14898045, essv14898040, essv14898106, essv14898039, essv14898075, essv14898078, essv14898060, essv14898114, essv14898102, essv14898090, essv14898053, essv14898048, essv14898043, essv14898104, essv14898041, essv14898076, essv14898056, essv14898110, essv14898099, essv14898042, essv14898098, essv14898037, essv14898105, essv14898089, essv14898109, essv14898069, essv14898116, essv14898073, essv14898088, essv14898083, essv14898120, essv14898091, essv14898092, essv14898071, essv14898058, essv14898112, essv14898068, essv14898107, essv14898087, essv14898077, essv14898044, essv14898050, essv14898080, essv14898061, essv14898074, essv14898059, essv14898065, essv14898057, essv14898052, essv14898062, essv14898079, essv14898115, essv14898118, essv14898055, essv14898108, essv14898046, essv14898097, essv14898049, essv14898063, essv14898086, essv14898047, essv14898095, essv14898113, essv14898066, essv14898081, essv14898103, essv14898085, essv14898101, essv14898072, essv14898054, essv14898117, essv14898111, essv14898067, essv14898093, essv14898070, essv14898119, essv14898096, essv14898051

Samples

NA12717, NA12842, HG01303, NA12286, HG00384, HG03589, HG01389, NA19020, NA20321, HG03999, HG01506, NA12812, HG00251, HG03873, NA20910, NA12761, HG00277, NA12005, HG01757, HG01072, HG00113, NA19722, NA19036, HG04047, HG00637, HG00323, HG01967, NA20755, HG03884, HG00739, HG00743, HG01699, HG01524, HG00349, HG00133, HG01183, HG03780, HG00266, HG01187, HG00332, HG00245, NA20505, NA18939, HG01142, HG00344, NA20767, HG00239, HG01619, HG03824, HG03625, NA19752, HG01334, HG02286, HG01680, HG00246, HG00126, HG01363, NA20872, HG01444, HG03866, HG02089, NA20801, NA19747, HG01131, HG03692, HG01685, HG00638, HG01396, NA20785, NA20527, HG01489, NA12347, HG02230, HG02235, HG01783, HG02113, NA11843, HG03922, HG02425, NA12154, HG03867, HG00554, NA11832, HG01516

Known Genes

Method

Sequencing

Analysis

Platform

Multiple platforms

Comments

Reference

1000_Genomes_Consortium_Phase_3

Pubmed ID

21293372

Accession Number(s)

esv3633551

Frequency

Sample Size	2504
Observed Gain	0
Observed Loss	84
Observed Complex	0
Frequency	n/a