Variant Details

Variant: esv3642984

Internal ID

7029753

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
	chr18:70286354..70288222	hg38	UCSC Ensembl
Inner	chr18:70286375..70288201	hg38	UCSC Ensembl
Outer	chr18:70286333..70288243	hg38	UCSC Ensembl
	chr18:67953590..67955458	hg19	UCSC Ensembl
Inner	chr18:67953611..67955437	hg19	UCSC Ensembl
Outer	chr18:67953569..67955479	hg19	UCSC Ensembl

Cytoband

18q22.2

Allele length

Assembly	Allele length
hg38	1869
hg19	1869

Variant Type

CNV loss

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

Merged Variants

Supporting Variants

essv15930808, essv15930822, essv15930784, essv15930895, essv15930835, essv15930888, essv15930791, essv15930787, essv15930873, essv15930841, essv15930887, essv15930849, essv15930829, essv15930855, essv15930810, essv15930823, essv15930832, essv15930875, essv15930871, essv15930799, essv15930824, essv15930870, essv15930866, essv15930881, essv15930850, essv15930790, essv15930858, essv15930838, essv15930804, essv15930851, essv15930884, essv15930820, essv15930825, essv15930798, essv15930869, essv15930836, essv15930839, essv15930794, essv15930816, essv15930821, essv15930886, essv15930815, essv15930837, essv15930842, essv15930802, essv15930792, essv15930817, essv15930801, essv15930795, essv15930891, essv15930852, essv15930844, essv15930857, essv15930803, essv15930834, essv15930896, essv15930863, essv15930865, essv15930830, essv15930785, essv15930786, essv15930872, essv15930788, essv15930833, essv15930789, essv15930878, essv15930893, essv15930847, essv15930826, essv15930861, essv15930812, essv15930800, essv15930819, essv15930862, essv15930796, essv15930867, essv15930864, essv15930828, essv15930843, essv15930814, essv15930805, essv15930885, essv15930889, essv15930806, essv15930894, essv15930813, essv15930846, essv15930856, essv15930818, essv15930793, essv15930797, essv15930848, essv15930882, essv15930879, essv15930890, essv15930897, essv15930868, essv15930874, essv15930892, essv15930859, essv15930883, essv15930876, essv15930845, essv15930854, essv15930831, essv15930860, essv15930880, essv15930807, essv15930853, essv15930809, essv15930840, essv15930877, essv15930827, essv15930898, essv15930811

Samples

HG01413, HG00304, HG00142, NA20766, NA10851, HG00351, HG00358, NA20783, NA11931, NA20802, HG00367, HG00103, NA12004, HG00364, NA12340, NA20332, HG01522, HG00327, HG00271, NA20814, HG01350, NA21135, HG01766, HG01492, NA11992, HG03874, NA20759, HG01455, HG00335, NA06984, HG01170, NA20812, HG00113, NA11994, NA19075, HG00182, HG01259, NA20811, HG00338, NA20764, HG01133, NA19445, HG00326, NA19789, NA20753, HG01524, HG00313, HG01136, HG00188, NA12489, HG01248, HG01360, HG00183, HG01200, HG01670, HG00145, NA19403, NA12342, NA20505, HG02090, HG00190, HG04195, HG00368, HG00239, HG03823, HG00373, NA20581, HG01182, HG01101, HG00321, HG00140, NA20282, HG00146, HG01708, HG03755, HG00099, NA12778, HG01697, NA12716, HG00285, NA19735, NA12775, HG02546, HG00353, HG00357, NA20870, HG02304, NA20785, HG01174, HG00308, NA20778, HG02274, HG00116, NA20281, HG00269, HG01577, HG01491, HG02230, HG01556, NA12749, HG02235, HG00342, NA12830, HG00343, HG00372, HG00274, HG00252, NA20886, NA20502, HG01111, HG00171, HG00345, HG01786, HG01583, HG01516

Known Genes

Method

Sequencing

Analysis

Platform

Multiple platforms

Comments

Reference

1000_Genomes_Consortium_Phase_3

Pubmed ID

21293372

Accession Number(s)

esv3642984

Frequency

Sample Size	2504
Observed Gain	0
Observed Loss	115
Observed Complex	0
Frequency	n/a