Variant Details

Variant: esv2665399

Internal ID

9931504

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
	chr1:45517815..45517911	hg38	UCSC Ensembl
	chr1:45983487..45983583	hg19	UCSC Ensembl

Cytoband

1p34.1

Allele length

Assembly	Allele length
hg38	97
hg19	97

Variant Type

CNV deletion

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

Merged Variants

Supporting Variants

essv6357745, essv5415381, essv6474979, essv5493372, essv5940814, essv6442783, essv5444094, essv6027874, essv5846014, essv6434040, essv5795500, essv5771757, essv6004628, essv5931180, essv6048592, essv6359849, essv6368407, essv6534166, essv5424962, essv5416347, essv6424655, essv5518594, essv5594186, essv6004723, essv6020515, essv6321479, essv6163197, essv6222718, essv6065485, essv6157053, essv5520867, essv5578441, essv6561270, essv6565445, essv5560844, essv5904607, essv6502756, essv5609027, essv5985920, essv6171252, essv6423857, essv6062192, essv5889407, essv6044866, essv5650897, essv5742154, essv6373353, essv6362642, essv5958537, essv6303639, essv5635715, essv5856784, essv6134248, essv5689009, essv6565005, essv5873219, essv6263842, essv6168533, essv5445839, essv5898824, essv5620233, essv5827803, essv5605624, essv6430177, essv6066844, essv6138218, essv5722832, essv5931653, essv6114117, essv5519851, essv6492148, essv6129913, essv5623640, essv5499702, essv6125446, essv6486543, essv5729321, essv6573960, essv5849975, essv5700874, essv5404656, essv5703078, essv6458326, essv6417312

Samples

NA12717, HG00442, NA11995, NA12414, HG01374, HG00699, NA19777, NA18530, NA19190, NA18870, NA18510, NA07357, NA18602, NA19107, HG01350, NA18940, NA18519, HG01351, NA18982, NA18942, NA18916, HG00346, NA18571, NA12287, NA19138, HG00311, NA18611, NA19404, NA12282, HG00335, NA19087, NA18990, NA18557, HG00260, NA10847, HG01353, HG00313, HG00137, HG00190, HG00475, HG00583, HG01498, HG00500, NA20126, NA18572, NA19654, HG00324, HG01073, NA19114, NA11919, NA19084, HG00404, NA20581, HG00276, HG00146, NA18963, NA18523, NA12778, NA18945, NA18542, NA19440, NA11881, NA18961, HG00375, HG00357, NA18941, NA19773, HG00308, HG00473, NA19428, HG00319, NA19085, HG00125, HG00111, NA19785, NA18609, HG00310, HG00252, NA19661, NA18612, NA18622, HG00553, NA18562, NA18577

Known Genes

PRDX1

Method

Merging

Analysis

No reference, merging analysis

Platform

Merging

Comments

Reference

1000_Genomes_Consortium_Phase_1

Pubmed ID

23128226

Accession Number(s)

esv2665399

Frequency

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