Variant CNV_M1_HG19_15_30916885_30992199
Location: chr15:30916885-30992199 (75Kb)
Site classification: Multi-allelic
Variant DCN frequency: 0.016
Genes Overlapped
Site classification: Multi-allelic
Variant DCN frequency: 0.016
Genes Overlapped
| ARHGAP11B | CDS | rho GTPase-activating protein 11B |
1000 Genomes Phase 1
Diploid copy number distribution
POP CN0 CN1 CN2 CN3
ASW 0 0 45 0
CEU 0 1 63 2
CHB 0 0 78 0
CHS 0 0 91 0
CLM 0 1 48 0
FIN 0 0 62 0
GBR 0 1 53 0
IBS 0 0 6 0
JPT 0 9 60 0
LWK 0 0 69 0
MXL 0 0 54 0
PUR 0 0 52 0
TSI 0 0 83 0
YRI 0 0 71 0
AFR 0 0 140 0
AFR+ 0 0 185 0
AMR 0 1 154 0
ASN 0 9 229 0
EUR 0 2 267 2
ALL 0 12 835 2
Diploid copy number distribution (95% confident)
POP CN0 CN1 CN2 CN3
ASW 0 0 45 0
CEU 0 1 63 2
CHB 0 0 78 0
CHS 0 0 91 0
CLM 0 1 48 0
FIN 0 0 62 0
GBR 0 1 53 0
IBS 0 0 6 0
JPT 0 9 60 0
LWK 0 0 69 0
MXL 0 0 54 0
PUR 0 0 52 0
TSI 0 0 83 0
YRI 0 0 71 0
AFR 0 0 140 0
AFR+ 0 0 185 0
AMR 0 1 154 0
ASN 0 9 229 0
EUR 0 2 267 2
ALL 0 12 835 2
Imputation spider plots: ASW CEU CHB CHS CLM FIN GBR IBS JPT LWK MXL PUR TSI YRI