Variant Details

Variant: nsv469958

Internal ID

15209831

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
Inner	chr11:55603544..55828837	hg38	UCSC Ensembl
Inner	chr11:55371020..55596313	hg19	UCSC Ensembl
Inner	chr11:55127596..55352889	hg18	UCSC Ensembl

Cytoband

11q11

Allele length

Assembly	Allele length
hg38	225294
hg19	225294
hg18	225294

Variant Type

CNV loss

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

Merged Variants

Supporting Variants

nssv546136, nssv546134, nssv546123, nssv546135, nssv546116, nssv546159, nssv546156, nssv546158, nssv546125, nssv546149, nssv546150, nssv546171, nssv546166, nssv546160, nssv546168, nssv546172, nssv546130, nssv546127, nssv546163, nssv546119, nssv546173, nssv546167, nssv546148, nssv546126, nssv546117, nssv546137, nssv546122, nssv546118, nssv546157, nssv546169, nssv546145, nssv546129, nssv546155, nssv546124, nssv546161, nssv546141, nssv546132, nssv546147, nssv546139, nssv546151, nssv546115, nssv546121, nssv546146, nssv546138, nssv546162, nssv546164, nssv546170, nssv546152, nssv546133, nssv546140, nssv546128, nssv546153, nssv546144, nssv546174

Samples

HGDP00880, HGDP01231, HGDP00576, HGDP00655, HGDP00654, HGDP01388, HGDP00614, HGDP00695, HGDP01263, HGDP00903, HGDP00632, HGDP01039, HGDP00686, HGDP01046, HGDP00930, HGDP00643, HGDP00867, HGDP01262, HGDP00789, HGDP00876, HGDP01358, HGDP00615, HGDP01418, HGDP00591, HGDP01387, HGDP00568, HGDP00696, HGDP00054, HGDP00620, HGDP00566, HGDP00978, HGDP00676, HGDP00564, HGDP00647, HGDP00874, HGDP00491, HGDP01223, HGDP00864, HGDP00570, HGDP01317, HGDP00697, HGDP00926, HGDP00602, HGDP00453, HGDP00543, HGDP00388, HGDP00913, HGDP00657, HGDP00694, HGDP01260, HGDP00572, HGDP01217, HGDP00940, HGDP00058

Known Genes

OR4C11, OR4C6, OR4P4, OR4S2, OR5D13, OR5D14, OR5D18, OR5L1, OR5L2

Method

SNP array

Analysis

We used the previously validated default quality control criteria, excluding samples with a log R ratio standard deviation of >0.28, a median B allele frequency of >0.55 or <0.45, or a B allele frequency drift of >0.002 (for more details see Wang et al. 2007). As the PennCNV algorithm is more sensitive and specific to CNVs covering greater numbers of SNPs in the HumanHap550 array, use of a minimum number of SNPs in CNV detection increases the reliability of CNV calls (with a consequent reduction in calls per individual). We set 10 SNPs as the minimum detection threshold in the algorithm.

Platform

Illumina HumanHap550 Genotyping BeadChip v3

Comments

Reference

Jakobsson_et_al_2008

Pubmed ID

18288195

Accession Number(s)

nsv469958

Frequency

Sample Size	443
Observed Gain	0
Observed Loss	54
Observed Complex	0
Frequency	n/a