Variant Details

Variant: esv3306062

Internal ID

15153010

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
	chr11:127071220..127071221	hg38	UCSC Ensembl
Inner	chr11:127071202..127071239	hg38	UCSC Ensembl
Outer	chr11:127071201..127071240	hg38	UCSC Ensembl
	chr11:126941115..126941116	hg19	UCSC Ensembl
Inner	chr11:126941097..126941134	hg19	UCSC Ensembl
Outer	chr11:126941096..126941135	hg19	UCSC Ensembl
	chr11:126446325..126446326	hg18	UCSC Ensembl
Inner	chr11:126446344..126446307	hg18	UCSC Ensembl
Outer	chr11:126446306..126446345	hg18	UCSC Ensembl

Cytoband

11q24.2

Allele length

Assembly	Allele length
hg38	294
hg19	294
hg18	294

Variant Type

CNV mobile element insertion

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

Merged Variants

Supporting Variants

essv7825839, essv7809587, essv7776319, essv7826726, essv7771554, essv7771361, essv7773528, essv7809986, essv7801077, essv7797635, essv7819899, essv7808816, essv7799541, essv7810573, essv7771839, essv7822045, essv7795492, essv7789966, essv7822860, essv7811625, essv7800841, essv7821324, essv7794610, essv7823390, essv7778805, essv7813147, essv7818688, essv7831658, essv7834350, essv7824394, essv7814189, essv7787173, essv7789021, essv7774816, essv7775164, essv7784088, essv7829249, essv7801999, essv7808508, essv7791237, essv7830208, essv7770855, essv7815897, essv7779670, essv7778241, essv7818231, essv7815647, essv7803050, essv7780368, essv7790511, essv7813758, essv7835568, essv7798164, essv7785177, essv7833943, essv7832107, essv7796412, essv7779959, essv7777048, essv7816825, essv7773816, essv7814575, essv7784024, essv7778067, essv7820454, essv7807120, essv7792487

Samples

NA18502, NA12717, NA18947, NA11829, NA18508, NA12814, NA10851, NA18980, NA18561, NA11920, NA11931, NA12751, NA18545, NA19190, NA18526, NA12750, NA07357, NA07346, NA18563, NA19005, NA18550, NA12812, NA12891, NA18547, NA18960, NA18942, NA11992, NA07347, NA12287, NA19138, NA18498, NA12761, NA11994, NA12815, NA19239, NA12828, NA18638, NA12878, NA12872, NA18516, NA18579, NA18948, NA18907, NA18537, NA19114, NA11894, NA18856, NA12892, NA18532, NA18570, NA18593, NA18945, NA12716, NA18909, NA19240, NA07051, NA07037, NA12763, NA18609, NA18505, NA19129, NA12006, NA07000, NA18522, NA12154, NA18562, NA18577

Known Genes

Method

Sequencing

Analysis

Platform

Roche 454

Comments

Reference

1000_Genomes_Consortium_Pilot_Project

Pubmed ID

20981092

Accession Number(s)

esv3306062

Frequency

Sample Size	185
Observed Gain	67
Observed Loss	0
Observed Complex	0
Frequency	n/a