The identification of CNVs can have several clinical implications:
Diagnosis: Accurate diagnosis of genetic disorders can be achieved through the detection of pathogenic CNVs. Prognosis: Understanding the type and location of CNVs can help predict the severity and progression of the disorder. Treatment Planning: Knowledge of CNVs can guide personalized treatment strategies, including medical, surgical, and therapeutic interventions. Genetic Counseling: Families can benefit from genetic counseling to understand the inheritance patterns, recurrence risks, and implications for future pregnancies.
