Local polydispersity is the term describing the variety of molecules present at the same retention volume in size exclusion chromatography (SEC) analysis. In the analysis of a linear homopolymer, local polydispersity is generally attributed to the effect of axial dispersion: it can cause molecular size variety (i.e., imperfect resolution) at each retention volume and thus local polydispersity in the molecular weight. In the analysis of polymer blends (copolymers and branched polymers), it is possible to have local polydispersity, even when the resolution is perfect, because molecules of different compositions (or degrees of branching) can have the same molecular size in solution. Conventional SEC interpretation assumes no local polydispersity if the axial dispersion effects are negligible. Three methods are currently available for detecting local polydispersity by using a combination of differential refractive index, light scattering, and viscometer detectors: the chromatogram comparison method, the conventional calibration curve comparison method, and the universal calibration comparison method. Here we experimentally assess these three methods using polymer blends and emphasize the chromatogram comparison method. All three are shown to be useful for assessing triple detector systems, but they are capable of detecting local polydispersity due to molecular heterogeneity only for very large differences in specific refractive index increments in the blend components.