Variant CNV_M1_HG19_2_165791841_165795951
Location: chr2:165791841-165795951 (4.1Kb)
Site classification: Duplication
Variant DCN frequency: 0.001
Genes Overlapped
Site classification: Duplication
Variant DCN frequency: 0.001
Genes Overlapped
| SLC38A11 | CDS | putative sodium-coupled neutral amino acid transporter 11 |
1000 Genomes Phase 1
Diploid copy number distribution
POP CN0 CN1 CN2 CN3
ASW 0 0 45 0
CEU 0 0 66 0
CHB 0 0 78 0
CHS 0 0 91 0
CLM 0 0 49 0
FIN 0 0 62 0
GBR 0 0 54 0
IBS 0 0 6 0
JPT 0 0 68 1
LWK 0 1 68 0
MXL 0 0 54 0
PUR 0 0 51 1
TSI 0 0 83 0
YRI 0 0 71 0
AFR 0 1 139 0
AFR+ 0 1 184 0
AMR 0 0 154 1
ASN 0 0 237 1
EUR 0 0 271 0
ALL 0 1 846 2
Diploid copy number distribution (95% confident)
POP CN0 CN1 CN2 CN3
ASW 0 0 45 0
CEU 0 0 66 0
CHB 0 0 78 0
CHS 0 0 91 0
CLM 0 0 49 0
FIN 0 0 62 0
GBR 0 0 54 0
IBS 0 0 6 0
JPT 0 0 68 1
LWK 0 0 68 0
MXL 0 0 52 0
PUR 0 0 51 0
TSI 0 0 82 0
YRI 0 0 71 0
AFR 0 0 139 0
AFR+ 0 0 184 0
AMR 0 0 152 0
ASN 0 0 237 1
EUR 0 0 270 0
ALL 0 0 843 1
Imputation spider plots: ASW CEU CHB CHS CLM FIN GBR IBS JPT LWK MXL PUR TSI YRI