Variant CNV_M1_HG19_9_14287649_14291261
Location: chr9:14287649-14291261 (3.6Kb)
Site classification: Deletion
Variant DCN frequency: 0.005
Genes Overlapped
Site classification: Deletion
Variant DCN frequency: 0.005
Genes Overlapped
| NFIB | INTRON | nuclear factor 1 B-type |
1000 Genomes Phase 1
Diploid copy number distribution
POP CN0 CN1 CN2 CN3
ASW 0 0 45 0
CEU 0 2 64 0
CHB 0 0 77 1
CHS 0 0 91 0
CLM 0 0 49 0
FIN 0 2 60 0
GBR 0 0 54 0
IBS 0 0 6 0
JPT 0 0 69 0
LWK 0 0 69 0
MXL 0 0 54 0
PUR 0 0 52 0
TSI 0 1 82 0
YRI 0 0 71 0
AFR 0 0 140 0
AFR+ 0 0 185 0
AMR 0 0 155 0
ASN 0 0 237 1
EUR 0 5 266 0
ALL 0 5 843 1
Diploid copy number distribution (95% confident)
POP CN0 CN1 CN2
ASW 0 0 45
CEU 0 2 64
CHB 0 0 77
CHS 0 0 91
CLM 0 0 49
FIN 0 1 60
GBR 0 0 53
IBS 0 0 6
JPT 0 0 69
LWK 0 0 68
MXL 0 0 54
PUR 0 0 52
TSI 0 1 82
YRI 0 0 71
AFR 0 0 139
AFR+ 0 0 184
AMR 0 0 155
ASN 0 0 237
EUR 0 4 265
ALL 0 4 841
Imputation spider plots: ASW CEU CHB CHS CLM FIN GBR IBS JPT LWK MXL PUR TSI YRI