The following links lead to initial questionnaires for each deletion we are studying. Please select below the region affected in your family. We will use these questionnaires to obtain some preliminary information about you and your family members who carry the rare deletion.

We estimate that the survey will take approximately 15 minutes to complete. We note that participation in the questionnaire is completely voluntary. All answers will be kept strictly confidential, and protected to the maximum extent as required by law.

After you complete the questionnaire, we will contact you directly with further information on our study. Your participation in this study will be very important in understanding the connections between genetic variants and the symptoms identified in individuals carrying rare deletions.

• 1q21.1 deletion questionnaire
• 15q13.3 deletion questionnaire
• 16p11.2 distal deletion questionnaire
• 16p12.2 deletion questionnaire
• 16p13.11 deletion questionnaire

If you have and questions about the terms used in this questionnaire or otherwise would like assistance completing it, please contact Dr. Girirajan by email at sxg47[at]psu.edu or by phone at (814) 865-0674.