Modest Impact on Risk for Autism Spectrum Disorder of Rare Copy Number Variants at 15q11.2, Specifically Breakpoints 1 to 2
Version of Record online: 12 MAY 2014
© 2014 International Society for Autism Research, Wiley Periodicals, Inc.
Volume 7, Issue 3, pages 355–362, June 2014
How to Cite
Chaste, P., Sanders, S. J., Mohan, K. N., Klei, L., Song, Y., Murtha, M. T., Hus, V., Lowe, J. K., Willsey, A. J., Moreno-De-Luca, D., Yu, T. W., Fombonne, E., Geschwind, D., Grice, D. E., Ledbetter, D. H., Lord, C., Mane, S. M., Martin, D. M., Morrow, E. M., Walsh, C. A., Sutcliffe, J. S., State, M. W., Martin, C. L., Devlin, B., Beaudet, A. L., Cook, E. H. and Kim, S.-J. (2014), Modest Impact on Risk for Autism Spectrum Disorder of Rare Copy Number Variants at 15q11.2, Specifically Breakpoints 1 to 2. Autism Res, 7: 355–362. doi: 10.1002/aur.1378
- Issue online: 20 JUN 2014
- Version of Record online: 12 MAY 2014
- Manuscript Accepted: 19 MAR 2014
- Manuscript Received: 24 OCT 2013
- Simons Foundation. Grant Number: SFARI 124827
- NIH. Grant Numbers: K23MH082883, R01HD065272, R01MH089390
- Fondamental Foundation
Appendix S1. Description of SAC and STC families included in the study.
Figure S1. Distribution of SRS scores. Fathers SRS scores: untransformed (left) and square root transformed (right).
Figure S2. Frequencies of transmitted vs. not transmitted CNVs in probands and siblings.
Table S1. List of probands (p1) excluded from the analyses.
Table S2. Inheritance of BP1-BP2 CNV in siblings and probands of ASD families.
Table S3. Transmission of BP1-BP2 CNVs.
Table S4. Effect of CNV on phenotype in parents and siblings estimated from multiple linear regression analysis.
Table S5. Effect of CNV on phenotype in probands estimated from multiple linear regression analysis.
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