Copy Number Variation (CNV) Atlas of Human Development

Overview

About this study

As a member of the ISCA Consortium, Mayo Cytogenetics Laboratory plans to contribute to the ISCA Clinical CNV Database by routinely submitting limited datasets of prospective patient genotype and phenotype information collected during routine clinical care. We will also utilize the database to improve reporting of clinical test results and to better advise clinicians as to the clinical significance of CNVs detected in their patients

Participation eligibility

Participant eligibility includes age, gender, type and stage of disease, and previous treatments or health concerns. Guidelines differ from study to study, and identify who can or cannot participate. There is no guarantee that every individual who qualifies and wants to participate in a trial will be enrolled. Contact the study team to discuss study eligibility and potential participation.

Inclusion Criteria:

Any individual who has clinical cytogenomic array testing through the Mayo Cytogenetics Laboratory.

Exclusion Criteria:

None

Participating Mayo Clinic locations

Study statuses change often. Please contact the study team for the most up-to-date information regarding possible participation.

Mayo Clinic Location	Status
Rochester, Minn. Mayo Clinic principal investigator Erik Thorland, Ph.D.	Closed for enrollment

Mayo Clinic Location

Status

Rochester, Minn.

Mayo Clinic principal investigator

Erik Thorland, Ph.D.

Closed for enrollment

More information

Publications

Publications are currently not available

Clinical Trials