Abstract 1452: Analyses of whole exome sequencing (WES) data of hereditary lung cancer families identify germline copy number variations (CNVs) in multiple genes von Waldron, John, Termine, Kirsten W., Musolf, Anthony M., de Andrade, Mariza, Gaba, Colette, Govindan, Ramaswamy, Yang, Ping, You, Ming, Jaeger, Ellen, Bencaz, Angelle F., Anderson, Marshall W., Schwartz, Ann G., Pinney, Susan M., Amos, Christopher I., Bailey-Wilson, Joan E., Mandal, Diptasri M.

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