A curated catalogue of human genomic structural variation

Variant Details

Variant: nsv553963

Internal ID

16341372

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
Inner	chr11:31372513..31375881	hg38	UCSC Ensembl
Inner	chr11:31394060..31397428	hg19	UCSC Ensembl
Inner	chr11:31350636..31354004	hg18	UCSC Ensembl

Cytoband

11p13

Allele length

Assembly	Allele length
hg38	3369
hg19	3369
hg18	3369

Variant Type

CNV loss

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

M

Merged Variants

Supporting Variants

nssv770955, nssv770816, nssv770926, nssv770952, nssv770771, nssv770813, nssv770942, nssv770767, nssv770866, nssv770939, nssv770902, nssv770920, nssv770868, nssv770787, nssv770825, nssv770794, nssv770741, nssv770880, nssv770898, nssv770899, nssv770841, nssv770757, nssv770755, nssv770944, nssv770856, nssv770954, nssv770925, nssv770948, nssv770732, nssv770855, nssv770727, nssv770796, nssv770817, nssv770903, nssv770739, nssv770849, nssv770792, nssv770886, nssv770872, nssv770753, nssv770724, nssv770829, nssv770938, nssv770851, nssv770913, nssv770754, nssv770752, nssv770836, nssv770751, nssv770858, nssv770764, nssv770802, nssv770863, nssv770830, nssv770828, nssv770934, nssv770723, nssv770867, nssv770837, nssv770758, nssv770798, nssv770919, nssv770780, nssv770894, nssv770805, nssv770895, nssv770818, nssv770909, nssv770949, nssv770810, nssv770735, nssv770820, nssv770725, nssv770847, nssv770746, nssv770961, nssv770923, nssv770910, nssv770729, nssv770809, nssv770747, nssv770877, nssv770726, nssv770763, nssv770897, nssv770760, nssv770749, nssv770928, nssv770728, nssv770833, nssv770769, nssv770857, nssv770933, nssv770957, nssv770870, nssv770750, nssv770871, nssv770854, nssv770807, nssv770876, nssv770765, nssv770797, nssv770875, nssv770776, nssv770756, nssv770815, nssv770835, nssv770853, nssv770788, nssv770960, nssv770777, nssv770861, nssv770768, nssv770869, nssv770834, nssv770891, nssv770827, nssv770785, nssv770935, nssv770936, nssv770803, nssv770921, nssv770916, nssv770734, nssv770812, nssv770918, nssv770865, nssv770864, nssv770783, nssv770881, nssv770804, nssv770793, nssv770883, nssv770932, nssv770744, nssv770937, nssv770838, nssv770799, nssv770915, nssv770736, nssv770941, nssv770772, nssv770874, nssv770859, nssv770914, nssv770911, nssv770737, nssv770848, nssv770826, nssv770940, nssv770781, nssv770778, nssv770908, nssv770950, nssv770892, nssv770873, nssv770840, nssv770819, nssv770775, nssv770824, nssv770901, nssv770740, nssv770731, nssv770742, nssv770945, nssv770917, nssv770842, nssv770930, nssv770862, nssv770786, nssv770907, nssv770905, nssv770789, nssv770850, nssv770738, nssv770759, nssv770888, nssv770887, nssv770822, nssv770893, nssv770927, nssv770832, nssv770806, nssv770801, nssv770878, nssv770839, nssv770779, nssv770884, nssv770766, nssv770800, nssv770882, nssv770900, nssv770770, nssv770896, nssv770846, nssv770748, nssv770959, nssv770791, nssv770890, nssv770843, nssv770761, nssv770845, nssv770773, nssv770745, nssv770947, nssv770814, nssv770956, nssv770951, nssv770924, nssv770953, nssv770808, nssv770733, nssv770790, nssv770795, nssv770784, nssv770831, nssv770782, nssv770774, nssv770929, nssv770762, nssv770931, nssv770811, nssv770958, nssv770889, nssv770860, nssv770943, nssv770743, nssv770922, nssv770904, nssv770906, nssv770821, nssv770912, nssv770879, nssv770730, nssv770885, nssv770946, nssv770852, nssv770844, nssv770823

Samples

Known Genes

Method

SNP array

Analysis

Illumina SNP array copy number analysis

Platform

Not reported

Comments

Reference

Cooper_et_al_2011

Pubmed ID

Accession Number(s)

Frequency

Sample Size	17421
Observed Gain	0
Observed Loss	239
Observed Complex	0
Frequency	n/a