View CNVs/SVs
View by Evidence Type: de novo CNVs (
CNVs Only Present In Patients
de novo CNVs
Overlapping/Recurrent CNVs
CNVs Overlapping With ACRD
CNVs Not Present In Control
Significant Enriched CNVs
Others
All
)
View by Chromosome:1 ( 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 X Y All )
Notes: ACRD: Autism Chromosome Rearrangement Database
| CNV Name | Chr | Band | Gain/Loss | Number of CNVs | Evidence Type | Reference | |
|---|---|---|---|---|---|---|---|
| Case | Control | ||||||
| AutCNV0005645 | 1 | 1 | - | - | - | de novo CNVs; | Krumm N, 2015 |
| AutCNV0005694 | 1 | - | Loss | - | - | CNVs Only Present In Patients; de novo CNVs; | Yuen RK, 2016 |
| AutCNV0005700 | 1 | - | Loss | - | - | CNVs Only Present In Patients; de novo CNVs; | C Yuen RK, 2017 |
| AutCNV0005874 | 1 | 1p36.32 | gain | - | - | de novo CNVs; | Brandler WM, 2018 |
| AutCNV0005875 | 1 | 1p36.22 | loss | - | - | de novo CNVs; | Brandler WM, 2018 |
| AutCNV0005876 | 1 | 1p32.3 | loss | - | - | de novo CNVs; | Brandler WM, 2018 |
| AutCNV0005877 | 1 | 1p22.2 | loss | - | - | de novo CNVs; | Brandler WM, 2018 |
| AutCNV0005878 | 1 | 1q23.3 | loss | - | - | de novo CNVs; | Brandler WM, 2018 |