Variant Details

Variant: esv2668092

Internal ID

9587511

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
Inner	chr14:89362422..89362478	hg38	UCSC Ensembl
Outer	chr14:89362051..89362848	hg38	UCSC Ensembl
Inner	chr14:89828766..89828822	hg19	UCSC Ensembl
Outer	chr14:89828395..89829192	hg19	UCSC Ensembl

Cytoband

14q32.11

Allele length

Assembly	Allele length
hg38	798
hg19	798

Variant Type

CNV deletion

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

Merged Variants

Supporting Variants

essv5876236, essv5874267, essv5812982, essv5641973, essv6217924, essv5966213, essv5763808, essv6596592, essv6025566, essv6184295, essv5934842, essv6060918, essv5902423, essv5908890, essv6094636, essv6592782, essv5624474, essv6334117, essv5862722, essv5804141, essv6329819, essv5569418, essv6057403, essv5976641, essv6406885, essv5988882, essv6542810, essv6158328, essv6247382, essv6505382, essv6524690, essv5504733, essv5775310, essv6171203, essv5668065, essv6205985, essv6106141, essv5931472, essv5962329, essv5690060, essv5406652, essv5668194, essv6500013, essv6032478, essv5874941, essv5965337, essv5929819, essv6462019, essv6088101, essv5627113, essv5645685, essv5538599, essv5930989, essv6008094, essv6329248, essv5992523, essv6408138, essv6133942, essv5768764, essv5851121, essv5646128, essv6421452, essv5546071, essv5990547, essv5498205, essv6408954, essv6543164, essv5682674, essv5802085, essv5629788, essv5855318, essv5690148, essv6090190, essv6466061, essv5985672, essv5808510, essv6329015, essv6548494, essv6334248, essv5703619, essv6289821, essv5748745, essv6030595, essv5549745, essv5892925, essv6222269, essv6524984, essv6198032, essv6333071, essv5475097, essv6128346, essv6228298, essv6074667, essv5679656, essv5857423, essv6219737, essv6488878, essv5588438, essv5579394, essv6235746

Samples

HG01441, NA19012, NA18964, NA18951, NA19081, NA18952, NA18975, NA19060, NA19003, NA19072, NA18948, HG01492, NA18953, NA18972, NA18947, NA19010, NA18963, NA19004, NA18965, NA19084, NA18943, NA18950, HG01171, HG00353, NA18596, NA18949, NA19077, HG00154, NA19062, HG01148, NA19067, NA19085, NA18967, NA19054, NA19059, NA19076, NA19057, NA19068, NA18536, NA18960, NA18990, NA19083, NA19088, NA18956, NA19066, NA18959, NA18976, NA18637, NA18973, NA19075, NA18982, NA19056, NA19082, NA19000, NA19055, NA19380, NA19080, NA19373, NA19384, NA18968, NA18986, NA19005, NA19002, NA18977, NA18941, NA18942, NA18961, NA18988, HG01070, NA19074, NA18910, NA18974, NA18985, NA19462, NA18945, NA18606, NA18940, NA18987, NA18999, NA18983, NA19078, NA19009, NA18989, NA18971, NA19755, NA19064, NA18944, NA19063, NA19070, NA18984, HG00693, NA11829, NA18981, NA19079, NA19087, NA19007, NA19065, NA19058, NA18980, HG01354

Known Genes

FOXN3

Method

Merging

Analysis

No reference, merging analysis

Platform

Merging

Comments

Reference

1000_Genomes_Consortium_Phase_1

Pubmed ID

23128226

Accession Number(s)

esv2668092

Frequency

Sample Size	1151
Observed Gain	0
Observed Loss	100
Observed Complex	0
Frequency	n/a